RecruitingPhase 2NCT05787327

RCT for Yinqiaosan-Maxingganshitang in the Treatment of COVID-19

Assessing the Efficacy and Safety of Yinqiaosan-Maxingganshitang in the Treatment of the Major Symptoms of Mild and Moderate COVID-19 by Telemedicine - a Randomized, Double-blind, Placebo-controlled Trial


Sponsor

Chinese University of Hong Kong

Enrollment

96 participants

Start Date

May 25, 2023

Study Type

INTERVENTIONAL

Conditions

Summary

This is a randomized, double-blinded, placebo-controlled clinical trial. This study is to evaluate the effectiveness and safety of Yinqiaosan-Maxingganshitang in the treatment of the major symptoms of mild and moderate COVID-19 patients by telemedicine.


Eligibility

Min Age: 18 YearsMax Age: 65 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a drug called Chinese Herb and Placebo for people with covid-19. The study is currently recruiting participants at 1 location. People eligible for this study include aged 18 Years to 65 Years.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGChinese Herb

Yinqiaosan-Maxingganshitang granules

DIAGNOSTIC_TESTPlacebo

Placebo


Locations(1)

Hong Kong Institute of Integrative Medicine

Hong Kong, Hong Kong

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NCT05787327


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