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  1. Article ; Online: The efficacy of oral Lavandula angustifolia Mill. essential oil on menopausal symptoms, serum lipid profile, and cortisol concentration in postmenopausal women: A triple-blind, randomized, controlled trial.

    Haramshahi, Morteza / Babaie, Soraya / Shahnazi, Mahnaz / Kafil, Behnam / Farshbaf-Khalili, Azizeh / Naghdi, Mina

    Complementary therapies in medicine

    2024  Volume 82, Page(s) 103050

    Abstract: Objective: To determine the effect of oral Lavandula angustifolia Mill. essential oil (LEO) on menopausal symptoms, serum cortisol level, and lipid profile in postmenopausal women.: Methods: This was a triple-blind parallel-armed randomized trial. ... ...

    Abstract Objective: To determine the effect of oral Lavandula angustifolia Mill. essential oil (LEO) on menopausal symptoms, serum cortisol level, and lipid profile in postmenopausal women.
    Methods: This was a triple-blind parallel-armed randomized trial. Seventy-two postmenopausal women aged 50-65 years referring to healthcare centers in Tabriz, Iran with a score of 15-42 on the Green scale were included from May 10, 2022 to May 22, 2023. The participants were randomly assigned to two groups with a 1:1 ratio and using four and six blocks. One group received LEO soft gel 80 mg per day, and another group received a similar placebo for 60 days. A demographic questionnaire and a Greene menopause symptom scale were used for data collection. The lipid profile (total cholesterol, triglyceride, LDL, HDL) and the serum levels of cortisol were measured using biochemical methods. Chi-square, Fisher's exact tests, Independent samples t-test, Analysis of Covariance (ANCOVA), Repeated measure ANOVA, and Paired sample t-test were utilized for analyses. A p-value less than 0.05 was considered statistically significant.
    Results: The demographic and personal characteristics of the participants were similar. After two months of intervention, all symptoms in psychological, physical, vasomotor, anxiety, depression, and sexual dysfunction domains were significantly relieved (decreased) among both groups (p < 0.003), except for sexual dysfunction, the reduction of which was not significant in the placebo group (p = 0.317). The mean (SD) total score of menopausal symptoms reduced from 27.4 (6.3) at baseline to 17.7 (4.9) at the end of the study in the LEO group (p < 0.001). It also decreased from 27.4 (7.1) to 17.6 (5.1) in the placebo group (p < 0.001). However, between-group analyses revealed that this reduction was significantly greater in the LEO group compared to the placebo group only in the sexual dysfunction (Mean (SD): 1.3 (0.6) vs. 1.0 (0.5); adjusted mean difference (95% confidence interval); p: - 0.35 (-0.67 to -0.02); 0.039). No significant within-group changes or between-group differences were observed (p > 0.05) in terms of studied serum markers.
    Conclusion: The oral LEO exhibited a significant enhancement in sexual dysfunction among postmenopausal women. Therefore, it can be used alongside other therapies to improve sexual dysfunction during menopause. LEO did not affect lipid profile and serum cortisol level in this study.
    Language English
    Publishing date 2024-05-15
    Publishing country Scotland
    Document type Journal Article
    ZDB-ID 1155895-7
    ISSN 1873-6963 ; 0965-2299
    ISSN (online) 1873-6963
    ISSN 0965-2299
    DOI 10.1016/j.ctim.2024.103050
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  2. Article ; Online: Insulin Receptor Substrates Regulation and Clinical Responses Following Vanadium-Enriched Yeast Supplementation in Obese Type 2 Diabetic Patients: a Randomized, Double-Blind, Placebo-Controlled Clinical Trial.

    Ghalichi, Faezeh / Saghafi-Asl, Maryam / Kafil, Behnam / Faghfouri, Amir Hossein / Jourshari, Mahtab Rajabi / Naserkiadeh, Amin Akbari / Ostadrahimi, Alireza

    Biological trace element research

    2023  Volume 201, Issue 11, Page(s) 5169–5182

    Abstract: Increasing evidence suggests that organic vanadium compounds are bioavailable and safe therapeutic agents with insulin-mimetic and insulin-enhancing features. The objective of the current study was to examine the effect of vanadium-enriched yeast (VEY) ... ...

    Abstract Increasing evidence suggests that organic vanadium compounds are bioavailable and safe therapeutic agents with insulin-mimetic and insulin-enhancing features. The objective of the current study was to examine the effect of vanadium-enriched yeast (VEY) supplementation on the gene expression level of insulin receptor substrates and clinical manifestations of obese type 2 diabetic mellitus (T2DM) patients. In this randomized, double-blind, placebo-controlled clinical trial, 44 obese T2DM patients were randomly allocated into either VEY (0.9 mg/day vanadium pentoxide) or placebo group for 12 weeks. The mRNA expression level of protein tyrosine phosphatase 1B (PTP1B), phosphatase and tensin homolog (PTEN), mitogen-activated protein kinase (MAPK), ribosomal protein S6 kinase (S6K), and nuclear factor kappa-light-chain-enhancer of activated B cells (NFƘB) genes in the peripheral blood mononuclear cells, serum levels of metabolic parameters, anthropometric indices, as well as the quality of life, and dietary intake were collected at pre- and post-intervention phases. Analysis of covariance was performed to obtain the corresponding effect size. Results showed that VEY administration significantly decreased anthropometric indices and glycemic parameters and increased insulin sensitivity after adjusting for potential covariates (p < 0.05), in comparison to the placebo group. Additionally, VEY supplementation was significantly effective on MAPK, PTP1B, and NFƘB gene expression level, compared to the placebo group. No significant changes were noticed for dietary intake, quality of life, and lipid profile in the VEY group, compared to the placebo group. Overall, VEY supplementation can be considered as a promising safe adjunct therapy for improving anthropometric indices and glycemic parameters in T2DM patients.
    MeSH term(s) Humans ; Vanadium/pharmacology ; Vanadium/therapeutic use ; Vanadium/metabolism ; Saccharomyces cerevisiae/metabolism ; Receptor, Insulin/metabolism ; Blood Glucose ; Leukocytes, Mononuclear/metabolism ; Quality of Life ; Insulin/metabolism ; Insulin Resistance ; Yeast, Dried ; Diabetes Mellitus, Type 2 ; Double-Blind Method ; Dietary Supplements
    Chemical Substances Vanadium (00J9J9XKDE) ; Receptor, Insulin (EC 2.7.10.1) ; Blood Glucose ; Insulin
    Language English
    Publishing date 2023-02-24
    Publishing country United States
    Document type Randomized Controlled Trial ; Journal Article
    ZDB-ID 445336-0
    ISSN 1559-0720 ; 0163-4984
    ISSN (online) 1559-0720
    ISSN 0163-4984
    DOI 10.1007/s12011-023-03604-4
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Possible therapeutic effects of boron citrate and oleoylethanolamide supplementation in patients with COVID-19: A pilot randomized, double-blind, clinical trial.

    Akbari, Neda / Ostadrahimi, Alireza / Tutunchi, Helda / Pourmoradian, Samira / Farrin, Nazila / Najafipour, Farzad / Soleimanzadeh, Hamid / Kafil, Behnam / Mobasseri, Majid

    Journal of trace elements in medicine and biology : organ of the Society for Minerals and Trace Elements (GMS)

    2022  Volume 71, Page(s) 126945

    Abstract: Background: The present study aimed to assess the therapeutic effects of boron citrate and oleoylethanolamide supplementation in patients with COVID-19.: Methods: Forty adult patients with a diagnosis of COVID-19 were recruited in the present study. ... ...

    Abstract Background: The present study aimed to assess the therapeutic effects of boron citrate and oleoylethanolamide supplementation in patients with COVID-19.
    Methods: Forty adult patients with a diagnosis of COVID-19 were recruited in the present study. Patients were randomized in a 1:1:1:1 allocation ratio to 1of 4 treatment groups: (A) 5 mg of boron citrate twice a day, (B) 200 mg of oleoylethanolamide twice a day, (C) both therapies, or (D) routine treatments without any study medications. At pre-and post-intervention phase, some clinical and biochemical parameters were assessed.
    Results: Supplementation with boron citrate alone or in combination with oleoylethanolamide significantly improved O2 saturation and respiratory rate (p < 0.01). At the end of the study, significant increases in white blood cell and lymphocyte count were observed in the boron citrate and combined groups (p < 0.001). Boron citrate supplementation led to a significant decrease in serum lactate dehydrogenase (p = 0.026) and erythrocyte sedimentation rate (p = 0.014), compared with other groups. Furthermore, boron citrate in combination with oleoylethanolamide resulted in a significant reduction in the high-sensitivity C-reactive protein and interleukin-1β concentrations (p = 0.031 and p = 0.027, respectively). No significant differences were found among four groups post-intervention, in terms of hemoglobin concentrations, platelet count, and serum interleukin-6 levels. At the end of the study, common symptoms of COVID-19 including cough, fatigue, shortness of breath, and myalgia significantly improved in the supplemented groups, compared to the placebo (p < 0.05).
    Conclusion: Supplementation with boron citrate alone or in combination with oleoylethanolamide could improve some clinical and biochemical parameters in COVID-19 patients.
    MeSH term(s) Adult ; Humans ; COVID-19 ; Boron ; SARS-CoV-2 ; Pilot Projects ; Double-Blind Method ; Dietary Supplements ; Citrates ; Treatment Outcome
    Chemical Substances oleoylethanolamide (1HI5J9N8E6) ; Boron (N9E3X5056Q) ; oleoyl ethanolamine ; Citrates
    Language English
    Publishing date 2022-02-12
    Publishing country Germany
    Document type Randomized Controlled Trial ; Journal Article
    ZDB-ID 1236267-0
    ISSN 1878-3252 ; 1611-602X ; 0946-672X
    ISSN (online) 1878-3252 ; 1611-602X
    ISSN 0946-672X
    DOI 10.1016/j.jtemb.2022.126945
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Oleoylethanolamide, A Bioactive Lipid Amide, as A Promising Treatment Strategy for Coronavirus/COVID-19.

    Ghaffari, Samad / Roshanravan, Neda / Tutunchi, Helda / Ostadrahimi, Alireza / Pouraghaei, Mahboub / Kafil, Behnam

    Archives of medical research

    2020  Volume 51, Issue 5, Page(s) 464–467

    Abstract: The current outbreak of COVID-19 (coronavirus) has been identified by World Health Organization (WHO) as a global pandemic. With the emergence of the COVID-19 virus and considering the lack of effective pharmaceutical treatment for it, there is an urgent ...

    Abstract The current outbreak of COVID-19 (coronavirus) has been identified by World Health Organization (WHO) as a global pandemic. With the emergence of the COVID-19 virus and considering the lack of effective pharmaceutical treatment for it, there is an urgent need to identify safe and effective drugs or potential adjuvant therapy in this regard. Bioactive lipids with an array of known health-promoting properties can be suggested as effective agents in alleviating acute respiratory stress induced by virus. The bioactive lipid amide, oleoylethanolamide (OEA), due to several distinctive homeostatic properties, including anti-inflammatory activities, modulation of immune response, and anti-oxidant effects can be considered as a novel potential pharmacological alternative for the management of COVID-19.
    MeSH term(s) Betacoronavirus/drug effects ; Betacoronavirus/immunology ; COVID-19 ; Coronavirus Infections/drug therapy ; Coronavirus Infections/epidemiology ; Coronavirus Infections/immunology ; Coronavirus Infections/pathology ; Endocannabinoids/pharmacology ; Endocannabinoids/therapeutic use ; Humans ; Inflammation/drug therapy ; Inflammation/immunology ; Inflammation/pathology ; Oleic Acids/pharmacology ; Oleic Acids/therapeutic use ; Pandemics ; Pneumonia, Viral/drug therapy ; Pneumonia, Viral/epidemiology ; Pneumonia, Viral/immunology ; Pneumonia, Viral/pathology ; SARS-CoV-2
    Chemical Substances Endocannabinoids ; Oleic Acids ; oleoylethanolamide (1HI5J9N8E6)
    Keywords covid19
    Language English
    Publishing date 2020-04-15
    Publishing country United States
    Document type Journal Article
    ZDB-ID 1156844-6
    ISSN 1873-5487 ; 0188-4409 ; 0188-0128
    ISSN (online) 1873-5487
    ISSN 0188-4409 ; 0188-0128
    DOI 10.1016/j.arcmed.2020.04.006
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Assessment of boron-containing compounds and oleoylethanolamide supplementation on the recovery trend in patients with COVID-19: A structured summary of a study protocol for a randomized controlled trial.

    Tutunchi, Helda / Mobasseri, Majid / Pourmoradian, Samira / Soleimanzadeh, Hamid / Kafil, Behnam / Akbari, Neda / Monshikarimi, Alireza / Ostadrahimi, Alireza

    Trials

    2020  Volume 21, Issue 1, Page(s) 890

    Abstract: Objectives: In this study, we investigate the effect of boron-containing compounds and oleoylethanolamide supplementation on the recovery trend in patients with COVID-19.: Trial design: The current study is a single-center, randomized, double-blind, ... ...

    Abstract Objectives: In this study, we investigate the effect of boron-containing compounds and oleoylethanolamide supplementation on the recovery trend in patients with COVID-19.
    Trial design: The current study is a single-center, randomized, double-blind, placebo-controlled clinical trial with parallel groups.
    Participants: The inclusion criteria include male and female patients≥18 years of age, with a confirmed diagnosis of SARS-CoV-2 infection via polymerase chain reaction (PCR) and/or antibody test and with written informed consent to participate in this trial. The exclusion criteria include regular use of any other supplement, severe and critical COVID-19 pneumonia, pregnancy and breastfeeding. This study is being conducted at Imam Reza Hospital, Tabriz University of Medical Sciences, Tabriz, Iran.
    Intervention and comparator: Patients are randomly assigned to four groups. The first group (A) will take one capsule containing 5 mg of boron compounds twice a day for two weeks. The second group (B) will take one capsule containing 200 mg oleoylethanolamide twice a day for two weeks. The third group (C) will take one capsule containing 5 mg boron compounds with 200 mg oleoylethanolamide twice a day for two weeks, and the fourth group (D) does not receive any additional treatment other than routine treatments. Boron-containing compounds and oleoylethanolamide capsules will be synthesized at Nutrition Research Center of Tabriz University of Medical Sciences.
    Main outcomes: The primary end point of this study is to investigate the recovery rate of clinical symptoms, including fever, dry cough, and fatigue, as well as preclinical features, including complete blood count (CBC), the erythrocyte sedimentation rate (ESR), C-reactive protein (CRP) profiles within two weeks of randomization.
    Randomisation: Patients are randomized into four equal groups in a parallel design (allocation ratio 1:1). A randomized block procedure is used to divide subjects into one of four treatment blocks (A, B, C, and D) by a computer-generated allocation schedule.
    Blinding (masking): The participants and investigators (enrolling, assessing, and analyzing) are blinded to the intervention assignments until the end of the study and data analysis.
    Numbers to be randomised (sample size): The calculated total sample size is 40 patients, with 10 patients in each group.
    Trial status: The protocol is Version 1.0, May 17, 2020. Recruitment began May 19, 2020, and is anticipated to be completed by October 19, 2020.
    Trial registration: This clinical trial has been registered by the title of "Assessment of boron-containing compounds and oleoylethanolamide supplementation on the recovery trend in Patients with COVID-19: A double-blind randomized placebo-controlled clinical trial" in the Iranian Registry of Clinical Trials (IRCT). The registration number is " IRCT20090609002017N35 ", https://www.irct.ir/trial/48058 . The registration date is 17 May 2020.
    Full protocol: The full protocol is attached as an additional file, accessible from the Trials website (Additional file 1). In the interest in expediting dissemination of this material, the familiar formatting has been eliminated; this Letter serves as a summary of the key elements of the full protocol.
    MeSH term(s) Administration, Oral ; Adult ; Betacoronavirus/drug effects ; Betacoronavirus/isolation & purification ; Boron Compounds/administration & dosage ; Boron Compounds/adverse effects ; COVID-19 ; Coronavirus Infections/diagnosis ; Coronavirus Infections/drug therapy ; Dietary Supplements ; Double-Blind Method ; Drug Monitoring/methods ; Drug Therapy, Combination/methods ; Endocannabinoids/administration & dosage ; Endocannabinoids/adverse effects ; Female ; Humans ; Iran ; Male ; Oleic Acids/administration & dosage ; Oleic Acids/adverse effects ; Pandemics ; Pneumonia, Viral/diagnosis ; Pneumonia, Viral/drug therapy ; Randomized Controlled Trials as Topic ; SARS-CoV-2 ; Trace Elements/administration & dosage ; Trace Elements/adverse effects ; Treatment Outcome
    Chemical Substances Boron Compounds ; Endocannabinoids ; Oleic Acids ; Trace Elements ; oleoylethanolamide (1HI5J9N8E6)
    Keywords covid19
    Language English
    Publishing date 2020-10-27
    Publishing country England
    Document type Clinical Trial Protocol ; Letter
    ZDB-ID 2040523-6
    ISSN 1745-6215 ; 1468-6694 ; 1745-6215
    ISSN (online) 1745-6215
    ISSN 1468-6694 ; 1745-6215
    DOI 10.1186/s13063-020-04820-2
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  6. Article: Oleoylethanolamide, A Bioactive Lipid Amide, as A Promising Treatment Strategy for Coronavirus/COVID-19

    Ghaffari, Samad / Roshanravan, Neda / Tutunchi, Helda / Ostadrahimi, Alireza / Pouraghaei, Mahboub / Kafil, Behnam

    Arch Med Res

    Abstract: The current outbreak of COVID-19 (coronavirus) has been identified by World Health Organization (WHO) as a global pandemic. With the emergence of the COVID-19 virus and considering the lack of effective pharmaceutical treatment for it, there is an urgent ...

    Abstract The current outbreak of COVID-19 (coronavirus) has been identified by World Health Organization (WHO) as a global pandemic. With the emergence of the COVID-19 virus and considering the lack of effective pharmaceutical treatment for it, there is an urgent need to identify safe and effective drugs or potential adjuvant therapy in this regard. Bioactive lipids with an array of known health-promoting properties can be suggested as effective agents in alleviating acute respiratory stress induced by virus. The bioactive lipid amide, oleoylethanolamide (OEA), due to several distinctive homeostatic properties, including anti-inflammatory activities, modulation of immune response, and anti-oxidant effects can be considered as a novel potential pharmacological alternative for the management of COVID-19.
    Keywords covid19
    Publisher WHO
    Document type Article
    Note WHO #Covidence: #115861
    Database COVID19

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  7. Article ; Online: Oleoylethanolamide, A Bioactive Lipid Amide, as A Promising Treatment Strategy for Coronavirus/COVID-19

    Ghaffari, Samad / Roshanravan, Neda / Tutunchi, Helda / Ostadrahimi, Alireza / Pouraghaei, Mahboub / Kafil, Behnam

    Archives of Medical Research

    2020  Volume 51, Issue 5, Page(s) 464–467

    Keywords General Medicine ; covid19
    Language English
    Publisher Elsevier BV
    Publishing country us
    Document type Article ; Online
    ZDB-ID 1156844-6
    ISSN 0188-4409 ; 0188-0128
    ISSN 0188-4409 ; 0188-0128
    DOI 10.1016/j.arcmed.2020.04.006
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  8. Article: Effects of sodium selenite and selenium-enriched yeast on cardiometabolic indices of patients with atherosclerosis: A double-blind randomized clinical trial study.

    Khabbaz Koche Ghazi, Mahdiyeh / Ghaffari, Samad / Naemi, Mohammad / Salehi, Rezvaniyeh / Taban Sadeghi, Mohammadreza / Barati, Meisam / Namazi Shabestari, Alireza / Kafil, Behnam / Mesri Alamdari, Naimeh / Soleimanzadeh, Hamid / Tarighat-Esfanjani, Ali / Roshanravan, Neda

    Journal of cardiovascular and thoracic research

    2021  Volume 13, Issue 4, Page(s) 314–319

    Abstract: Introduction: ...

    Abstract Introduction:
    Language English
    Publishing date 2021-12-05
    Publishing country Iran
    Document type Journal Article
    ZDB-ID 2654729-6
    ISSN 2008-6830 ; 2008-5117
    ISSN (online) 2008-6830
    ISSN 2008-5117
    DOI 10.34172/jcvtr.2021.51
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  9. Article ; Online: A comprehensive systematic review of the effectiveness of

    Roshanravan, Neda / Bastani, Sepideh / Tutunchi, Helda / Kafil, Behnam / Nikpayam, Omid / Mesri Alamdari, Naimeh / Hadi, Amir / Sotoudeh, Simin / Ghaffari, Samad / Ostadrahimi, Alireza

    Archives of physiology and biochemistry

    2021  Volume 129, Issue 3, Page(s) 741–751

    Abstract: Aims and background: Obesity is recognised as a significant public health burden worldwide. Recently the cross-talk between gut microbiota and obesity has attracted much attention. To that end, : Methods: Electronic databases of MEDLINE, PubMed, ... ...

    Abstract Aims and background: Obesity is recognised as a significant public health burden worldwide. Recently the cross-talk between gut microbiota and obesity has attracted much attention. To that end,
    Methods: Electronic databases of MEDLINE, PubMed, Scopus, Web of Science, and Google Scholar were searched thought March 2020 to identify relevant published articles, and eligible articles were systematically reviewed.
    Results and conclusions: Fifteen studies were included in the present study. Findings from the present review, which included human and animal (rodent) models support the effectiveness of
    MeSH term(s) Gastrointestinal Microbiome ; Obesity/microbiology ; Obesity/therapy ; Metabolic Diseases/microbiology ; Metabolic Diseases/therapy ; Humans ; Animals ; Probiotics/therapeutic use ; Akkermansia ; Diet
    Language English
    Publishing date 2021-01-15
    Publishing country England
    Document type Review ; Journal Article ; Systematic Review
    ZDB-ID 1238320-x
    ISSN 1744-4160 ; 1381-3455
    ISSN (online) 1744-4160
    ISSN 1381-3455
    DOI 10.1080/13813455.2021.1871760
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  10. Article: Assessment of boron-containing compounds and oleoylethanolamide supplementation on the recovery trend in patients with COVID-19: A structured summary of a study protocol for a randomized controlled trial

    Tutunchi, Helda / Mobasseri, Majid / Pourmoradian, Samira / Soleimanzadeh, Hamid / Kafil, Behnam / Akbari, Neda / Monshikarimi, Alireza / Ostadrahimi, Alireza

    Trials

    Abstract: OBJECTIVES: In this study, we investigate the effect of boron-containing compounds and oleoylethanolamide supplementation on the recovery trend in patients with COVID-19. TRIAL DESIGN: The current study is a single-center, randomized, double-blind, ... ...

    Abstract OBJECTIVES: In this study, we investigate the effect of boron-containing compounds and oleoylethanolamide supplementation on the recovery trend in patients with COVID-19. TRIAL DESIGN: The current study is a single-center, randomized, double-blind, placebo-controlled clinical trial with parallel groups. PARTICIPANTS: The inclusion criteria include male and female patients≥18 years of age, with a confirmed diagnosis of SARS-CoV-2 infection via polymerase chain reaction (PCR) and/or antibody test and with written informed consent to participate in this trial. The exclusion criteria include regular use of any other supplement, severe and critical COVID-19 pneumonia, pregnancy and breastfeeding. This study is being conducted at Imam Reza Hospital, Tabriz University of Medical Sciences, Tabriz, Iran. INTERVENTION AND COMPARATOR: Patients are randomly assigned to four groups. The first group (A) will take one capsule containing 5 mg of boron compounds twice a day for two weeks. The second group (B) will take one capsule containing 200 mg oleoylethanolamide twice a day for two weeks. The third group (C) will take one capsule containing 5 mg boron compounds with 200 mg oleoylethanolamide twice a day for two weeks, and the fourth group (D) does not receive any additional treatment other than routine treatments. Boron-containing compounds and oleoylethanolamide capsules will be synthesized at Nutrition Research Center of Tabriz University of Medical Sciences. MAIN OUTCOMES: The primary end point of this study is to investigate the recovery rate of clinical symptoms, including fever, dry cough, and fatigue, as well as preclinical features, including complete blood count (CBC), the erythrocyte sedimentation rate (ESR), C-reactive protein (CRP) profiles within two weeks of randomization. RANDOMISATION: Patients are randomized into four equal groups in a parallel design (allocation ratio 1:1). A randomized block procedure is used to divide subjects into one of four treatment blocks (A, B, C, and D) by a computer-generated allocation schedule. BLINDING (MASKING): The participants and investigators (enrolling, assessing, and analyzing) are blinded to the intervention assignments until the end of the study and data analysis. NUMBERS TO BE RANDOMISED (SAMPLE SIZE): The calculated total sample size is 40 patients, with 10 patients in each group. TRIAL STATUS: The protocol is Version 1.0, May 17, 2020. Recruitment began May 19, 2020, and is anticipated to be completed by October 19, 2020. TRIAL REGISTRATION: This clinical trial has been registered by the title of "Assessment of boron-containing compounds and oleoylethanolamide supplementation on the recovery trend in Patients with COVID-19: A double-blind randomized placebo-controlled clinical trial" in the Iranian Registry of Clinical Trials (IRCT). The registration number is " IRCT20090609002017N35 ", https://www.irct.ir/trial/48058 . The registration date is 17 May 2020. FULL PROTOCOL: The full protocol is attached as an additional file, accessible from the Trials website (Additional file 1). In the interest in expediting dissemination of this material, the familiar formatting has been eliminated; this Letter serves as a summary of the key elements of the full protocol.
    Keywords covid19
    Publisher WHO
    Document type Article
    Note WHO #Covidence: #895024
    Database COVID19

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