Effects of Iranian herbal Zofa® syrup for the management of clinical symptoms in patients with COVID-19: A randomized clinical trial

Objective: The objective of this study was to determine the role of Iranian herbal Zofa® syrup in improving the clinical symptoms of patients with COVID-19.Materials and Methods: This randomized clinical trial was conducted on 105 patients with COVID-19. Patients were randomly assigned to the interv...

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সংরক্ষণ করুন:
গ্রন্থ-পঞ্জীর বিবরন
প্রধান লেখক: Ali Ghazvini (Author), Amir Vahedian-azimi (Author), Morteza Abdoli (Author), Farshid Rahimibashar (Author), Yunes Panahi (Author), Thozhukat Sathyapalan (Author), Amirhossein Sahebkar (Author)
বিন্যাস: গ্রন্থ
প্রকাশিত: Mashhad University of Medical Sciences, 2023-09-01T00:00:00Z.
বিষয়গুলি:
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001 doaj_8eeb0876960e42c6bc2a05b78fb76e9b
042 |a dc 
100 1 0 |a Ali Ghazvini  |e author 
700 1 0 |a Amir Vahedian-azimi  |e author 
700 1 0 |a Morteza Abdoli  |e author 
700 1 0 |a Farshid Rahimibashar  |e author 
700 1 0 |a Yunes Panahi  |e author 
700 1 0 |a Thozhukat Sathyapalan  |e author 
700 1 0 |a Amirhossein Sahebkar  |e author 
245 0 0 |a Effects of Iranian herbal Zofa® syrup for the management of clinical symptoms in patients with COVID-19: A randomized clinical trial 
260 |b Mashhad University of Medical Sciences,   |c 2023-09-01T00:00:00Z. 
500 |a 2228-7930 
500 |a 2228-7949 
500 |a 10.22038/ajp.2023.21909 
520 |a Objective: The objective of this study was to determine the role of Iranian herbal Zofa® syrup in improving the clinical symptoms of patients with COVID-19.Materials and Methods: This randomized clinical trial was conducted on 105 patients with COVID-19. Patients were randomly assigned to the intervention (n=35) group (received 10 ml of Zofa® syrup every 8 hours/seven days plus standard treatment) or the control (n=70) group (received only standard treatment). Assessments were performed before and after treatment.Results: The groups were comparable regarding age (p=0.980), gender (p=0.584), comorbidities (p=0.318), or drug history (p=0.771). There was no difference between patients' recovery status at the time of discharge (p=0.327) or two weeks post-discharge (p=0.165) in the intervention and control groups. No patient was hospitalized to the intensive care unit (ICU) for supplemental oxygen therapy and no patient died in the intervention group. However, in the control group, three (4.5%) patients were transferred to the ICU, and two (3.03%) patients died.Conclusion: Considering the better recovery status of the patients at the time of discharge and the absence of patient deaths in the intervention group, more additional studies are needed to confirm these findings and elucidate the role of Zofa® in COVID-19. 
546 |a EN 
690 |a coronavirus disease 2019 
690 |a herbal medicine 
690 |a respiratory infection 
690 |a symptoms 
690 |a iran 
690 |a Therapeutics. Pharmacology 
690 |a RM1-950 
655 7 |a article  |2 local 
786 0 |n Avicenna Journal of Phytomedicine, Vol 13, Iss 5, Pp 500-512 (2023) 
787 0 |n https://ajp.mums.ac.ir/article_21909_be6dfcf2cabe1232fa5cb84d506116e7.pdf 
787 0 |n https://doaj.org/toc/2228-7930 
787 0 |n https://doaj.org/toc/2228-7949 
856 4 1 |u https://doaj.org/article/8eeb0876960e42c6bc2a05b78fb76e9b  |z Connect to this object online.