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Evaluation of berberine pellet effect on clinical recovery time in COVID-۱۹ outpatients: A pilot clinical trial

عنوان مقاله: Evaluation of berberine pellet effect on clinical recovery time in COVID-۱۹ outpatients: A pilot clinical trial
شناسه ملی مقاله: JR_AJP-13-3_005
منتشر شده در در سال 1402
مشخصات نویسندگان مقاله:

Soodabeh Omidvar Tehrani - School of Pharmacy, Mashhad University of Medical Sciences, Mashhad, Iran
Mahboobeh Ghasemzadeh Rahbardar - Pharmaceutical Research Center, Pharmaceutical Technology Institute, Mashhad University of Medical Sciences, Mashhad, Iran
Kamran Shoorgashti - School of Pharmacy, Mashhad University of Medical Sciences, Mashhad, Iran
Mohammad Javad Dehghan Nayeri - Infection Control & Hand Hygiene Research Center, Mashhad University of Medical Sciences, Mashhad, Iran
Amir Hooshang Mohammadpour - Department of Clinical Pharmacy, School of Pharmacy, Mashhad University of Medical Sciences, Mashhad, Iran
Hossein Hosseinzadeh - Department of Pharmacodynamics and Toxicology, School of Pharmacy, Mashhad University of Medical Sciences, Mashhad, Iran

خلاصه مقاله:
Objective: Severe disease onset of COVID-۱۹ may result in alveolar injury and respiratory failure. Apoptosis and inflammation are the main causes of respiratory distress syndrome. Berberine is used in medicine as an analgesic, anti-asthmatic, anti-inflammatory, and antiviral. In the current investigation, the effect of berberine on COVID-۱۹ outpatients was studied.Materials and Methods: The present clinical trial was performed on ۴۰ outpatients who were randomly assigned to berberine (۳۰۰ mg, TID, ۲ weeks) (n=۱۹) or placebo groups (n=۲۱). Both groups received standard therapy and they were monitored on days ۳, ۷, and ۱۴ after the beginning of the therapy for clinical symptoms’ improvement, quantitative CRP, lymphopenia, CBC, and SpO۲. The severity and frequency of these symptoms and the level of the parameters were statistically compared between the two groups.Results: On days (۰, ۳, ۷, and ۱۴, there was no significant difference between the berberine and placebo groups in the improvement of clinical symptoms (cough, shortness of breath, nausea, loss of smell and taste, diarrhea, dizziness, sore throat, stomachache, body aches, and body temperature), quantitative CRP, lymphopenia, WBC, neutrophils, platelets, or SpO۲.Conclusion: Berberine (۳۰۰ mg, TID, two weeks) is ineffective in treating COVID-۱۹. More research with a larger sample size is needed to investigate different berberine dosages in other pharmaceutical formulations.

کلمات کلیدی:
Clinical trial, Berberis vulgaris, Barberry, Coronavirus disease, Lymphopenia, Antiviral

صفحه اختصاصی مقاله و دریافت فایل کامل: https://civilica.com/doc/1640327/