Shirvani Maria, Vaziri Siavash, Akrami Mohammad Reza, Sarmasti Azar, Hassanpour Kamyab, Akrami Ali
Department of Infectious Diseases, Kermanshah University of Medical Sciences, Kermanshah, Iran.
Department of Neurosurgery, Kermanshah University of Medical Sciences, Kermanshah, Iran.
Heliyon. 2024 Feb 19;10(5):e26685. doi: 10.1016/j.heliyon.2024.e26685. eCollection 2024 Mar 15.
Coronavirus disease 2019 (COVID-19) is still a global health issue with no certain treatment option. So far, various treatments have been suggested among which one can mention isotretinoin. The aim of the present study was to investigate the potential of this medication as a side treatment for COVID-19. This open-label controlled clinical trial with the approval ID of IRCT20190624043993N3 was conducted in Farabi Hospital, Kermanshah University of Medical Sciences, Kermanshah, Iran. Considering the inclusion and exclusion criteria, 52 patients diagnosed with COVID-19 were enrolled. The control group only received standard of care (SOC) treatment while the intervention arm received 40 mg per day of isotretinoin along with the SOC. The patients were followed until discharge. The results showed no death among the groups. The hospitalization duration in the intervention and SOC groups were 5.1 ± 2.29 and 5.1 ± 3.44 days, respectively with no statistical difference (P = 0.98). Moreover, the SpO, pulse rate, respiratory rate, and blood pressure also showed no statistical difference neither at admission nor upon discharge (P > 0.05). The laboratory investigations showed that white blood cells, absolute lymphocyte count, hemoglobin value, and platelet count did not differ between the groups at admission or upon discharge (P > 0.05). According to the results, it seems that isotretinoin didn't act as a potent side therapy in patients with COVID-19. However, due to the small sample size, we suggest further investigations.
2019冠状病毒病(COVID - 19)仍是一个尚无确定治疗方案的全球健康问题。到目前为止,已提出了各种治疗方法,其中可以提及异维甲酸。本研究的目的是调查这种药物作为COVID - 19辅助治疗的潜力。这项开放标签对照临床试验的批准号为IRCT20190624043993N3,在伊朗克尔曼沙赫医科大学法拉比医院进行。根据纳入和排除标准,招募了52名确诊为COVID - 19的患者。对照组仅接受标准治疗(SOC),而干预组在接受SOC的同时,每天服用40毫克异维甲酸。对患者进行随访直至出院。结果显示两组均无死亡病例。干预组和SOC组的住院时间分别为5.1±2.29天和5.1±3.44天,无统计学差异(P = 0.98)。此外,SpO、脉搏率、呼吸率和血压在入院时和出院时也均无统计学差异(P>0.05)。实验室检查表明,两组患者入院时和出院时的白细胞、绝对淋巴细胞计数、血红蛋白值和血小板计数均无差异(P>0.05)。根据结果,异维甲酸似乎对COVID - 19患者并非有效的辅助治疗药物。然而,由于样本量小,我们建议进一步研究。