Department of Psychiatry, Psychiatry and Behavioral Sciences Research Center, Addiction Institute, Mazandaran University of Medical Sciences, Sari, Iran.
Gastrointestinal Cancer Research Center, Non-Communicable Diseases Institute, Mazandaran University of Medical Sciences, Sari, Iran.
J Med Virol. 2022 Jan;94(1):263-271. doi: 10.1002/jmv.27312. Epub 2021 Sep 8.
This trial aims to evaluate the effectiveness of adding melatonin to the treatment protocol of hospitalized coronavirus disease 2019 (COVID-19) patients. This was an open-label, randomized controlled clinical trial in hospitalized COVID-19 patients. Patients were randomized into a treatment arm receiving melatonin plus standard care or a control arm receiving standard care alone. The trial's primary endpoint was sleep quality examined by the Leeds Sleep Evaluation Questionnaire (LSEQ). The trial's secondary endpoints were symptoms alleviation by Day 7, intensive care unit admission, 10-day mortality, white blood cell count, lymphocyte count, C-reactive protein status, and peripheral capillary oxygen saturation. Ninety-six patients were recruited and allocated to either the melatonin arm (n = 48) or control arm (n = 48). Baseline characteristics were similar across treatment arms. There was no significant difference in symptoms on Day 7. The mean of the LSEQ scores was significantly higher in the melatonin group (p < 0.001). There was no significant difference in laboratory data, except for blood oxygen saturation, which has improved significantly in the melatonin group compared with the control group (95.81% vs. 93.65% respectively, p = 0.003). This clinical trial study showed that the combination of oral melatonin tablets and standard treatment could substantially improve sleep quality and blood oxygen saturation in hospitalized COVID-19 patients.
这项试验旨在评估在住院的 2019 冠状病毒病(COVID-19)患者的治疗方案中添加褪黑素的效果。这是一项针对住院 COVID-19 患者的开放性、随机对照临床试验。患者被随机分配到接受褪黑素加标准治疗的治疗组或接受单独标准治疗的对照组。试验的主要终点是通过利兹睡眠评估问卷(LSEQ)评估的睡眠质量。试验的次要终点是第 7 天症状缓解、入住重症监护病房、10 天死亡率、白细胞计数、淋巴细胞计数、C 反应蛋白状态和外周毛细血管血氧饱和度。共招募了 96 名患者,并将其分配到褪黑素组(n = 48)或对照组(n = 48)。治疗组之间的基线特征相似。第 7 天的症状没有显著差异。褪黑素组的 LSEQ 评分平均值明显更高(p < 0.001)。实验室数据除了血氧饱和度外没有显著差异,褪黑素组与对照组相比血氧饱和度明显改善(分别为 95.81%和 93.65%,p = 0.003)。这项临床试验研究表明,口服褪黑素片联合标准治疗可显著改善住院 COVID-19 患者的睡眠质量和血氧饱和度。