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传统越南医学科威胶囊治疗非重症 COVID-19 患者:一项 III 期双盲随机对照试验。

Traditional Vietnamese medicine Kovir capsule for non-severe COVID-19 patients: A phase III double-blind randomized controlled trial.

机构信息

Traditional Medicine Institute of Ho Chi Minh City, Ho Chi Minh City, Vietnam.

Hanoi General Hospital for Traditional Medicine, Hanoi, Vietnam.

出版信息

Phytother Res. 2023 Jun;37(6):2395-2404. doi: 10.1002/ptr.7761. Epub 2023 Feb 7.

DOI:10.1002/ptr.7761
PMID:36751127
Abstract

The number of COVID-19 infections is still increasing with the omicron variant. Although vaccination has shown its effectiveness, efficacious treatments are still required. Kovir, a Vietnamese herbal medicine, has shown potential effects for non-severe COVID-19 patients in terms of symptom resolution and prevention of disease progression in previous studies. This phase-3 trial evaluated the safety and efficacy of Kovir for non-severe COVID-19 adults. Participants were randomized to the Kovir (381 patients) or placebo (192 patients) groups. Outcomes were progression to severe/critical COVID-19, a daily symptom score based on 11 pre-defined symptoms, time to symptom resolution, a negative reverse transcription polymerase chain reaction, an EQ-5D-5L quality of life (QOL) score, and serious adverse events. Only one patient (in the placebo group) progressed to severe COVID-19, thus we could not conclude the effect of Kovir on the prevention of disease progression. Kovir significantly reduced time to symptom resolution (median: 7 vs. 11 days, hazard ratio [95% confidence interval]: 2.03 [1.66-2.48]) compared to placebo. Kovir also increased the QOL score on days 7 and 14. No safety concerns were observed. To conclude, Kovir is safe and facilitates symptom relief for non-severe COVID-19 patients. We advocate using Kovir in the early phase of COVID-19 for non-severe adult patients.

摘要

奥密克戎变异株流行期间,COVID-19 感染人数仍在增加。虽然疫苗接种已显示出其有效性,但仍需要有效的治疗方法。科维尔(Kovir)是一种越南草药,在既往研究中显示出对非重症 COVID-19 患者在症状缓解和预防疾病进展方面的潜在效果。这项 3 期试验评估了科维尔治疗非重症 COVID-19 成人患者的安全性和有效性。参与者被随机分配到科维尔(381 例)或安慰剂(192 例)组。主要结局为进展为重症/危重症 COVID-19,基于 11 项预先定义的症状的每日症状评分,症状缓解时间,逆转录聚合酶链反应(RT-PCR)阴性,EQ-5D-5L 生活质量(QOL)评分,以及严重不良事件。仅有 1 例患者(安慰剂组)进展为重症 COVID-19,因此我们无法得出科维尔对预防疾病进展的效果。与安慰剂相比,科维尔显著缩短了症状缓解时间(中位数:7 天 vs. 11 天,风险比[95%置信区间]:2.03[1.66-2.48])。科维尔还增加了第 7 天和第 14 天的 QOL 评分。未观察到安全性问题。总之,科维尔安全且可缓解非重症 COVID-19 患者的症状。我们提倡在 COVID-19 的早期阶段对非重症成年患者使用科维尔。

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