The Efficacy of Colchicine as an Adjunct Therapy in Non-hospitalized COVID-19 Patients: A Randomized Placebo-Controlled Trial.

Sepideh Hejazi, Zohreh Jahani, Sepideh Elyasi, Davoud Salarbashi, Mona Kabiri
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Abstract

Background: The therapeutic potential of oral colchicine administration may help combat COVID-19 infection due to reduced disease severity and mortality risk.

Objective: This randomized trial aimed to assess the effect of colchicine treatment on the inflammatory and hematologic markers as well as clinical features in non-hospitalized patients with mild-to-moderate COVID-19 disease.

Methods: In the present placebo-controlled randomized trial, 80 non-hospitalized COVID-19 patients were enrolled and followed for 14 days. Subjects randomly received oral colchicine or placebo tablets once a day for two weeks. The fever and cough clinical signs, as well as Creactive protein (CRP) and lymphopenia, were evaluated through the follow-up.

Results: No significant between-group differences were observed in terms of the duration of clinical symptoms, CRP, and lymphopenia at 0, 7, and 14 days of intervention. Although the proportion of participants with fever, cough, positive CRP, and lymphopenia was higher reduced in the colchicine group than the placebo during treatment, no significant differences were found between groups. Due to no adverse effects detected in this trial, colchicine therapy was well-tolerated and safe.

Conclusion: Our findings revealed that colchicine adjuvant therapy had no beneficial effect on clinical and para-clinical parameters in non-hospitalized COVID-19 patients during 14 days of intervention. The present trial does not support colchicine as a potential treatment against COVID-19 disease.

秋水仙碱作为辅助疗法对非住院 COVID-19 患者的疗效:随机安慰剂对照试验。
背景:口服秋水仙碱的治疗潜力可能有助于对抗COVID-19感染,因为它可以降低疾病的严重程度和死亡风险:本随机试验旨在评估秋水仙碱治疗对轻度至中度COVID-19非住院患者的炎症和血液学指标以及临床特征的影响:在本安慰剂对照随机试验中,共招募了80名未住院的COVID-19患者,并对其进行了为期14天的随访。受试者随机口服秋水仙碱或安慰剂片剂,每天一次,连续两周。随访期间评估了发热和咳嗽的临床症状以及克雷反应蛋白(CRP)和淋巴细胞减少症:结果:在干预的 0、7 和 14 天内,临床症状、CRP 和淋巴细胞减少的持续时间在组间无明显差异。虽然在治疗过程中,秋水仙碱组出现发热、咳嗽、CRP 阳性和淋巴细胞减少的比例高于安慰剂组,但组间无明显差异。由于本试验未发现任何不良反应,因此秋水仙碱治疗的耐受性和安全性良好:我们的研究结果表明,秋水仙碱辅助治疗对未住院的 COVID-19 患者在 14 天的干预期间的临床和辅助临床指标无益处。本试验不支持将秋水仙碱作为治疗 COVID-19 疾病的潜在药物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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