# Efficacy of Shen Cao Gan Jiang Tang on Non-severe COVID-19 Patients: A Multicenter, Randomized, Open-Label Clinical Trial

**Authors:** Dieu-Thuong Thi Trinh, An Hoa Tran, Minh-Man Pham Bui, Thy Xuan Kieu, Van-Dan Nguyen, Nguyen Huu Lac Thuy, Khac-Minh Thai, Nguyen Lam Vuong

PMC · DOI: 10.7759/cureus.62380 · 2024-06-14

## TL;DR

A Vietnamese herbal formula called Shen Cao Gan Jiang Tang may help speed recovery in non-severe COVID-19 patients.

## Contribution

This study provides clinical evidence for the efficacy and safety of Shen Cao Gan Jiang Tang in treating non-severe COVID-19.

## Key findings

- SCGJT reduced symptom resolution time from 13 to 9 days compared to standard care.
- SCGJT decreased the need for symptomatic medications and hastened viral clearance.
- No adverse events were reported in patients using SCGJT.

## Abstract

Background

In the face of the escalating COVID-19 pandemic amid shortages of medications and vaccines, a Vietnamese herbal formula known as Shen Cao Gan Jiang Tang (SCGJT) has been put into use for non-severe COVID-19 patients. This study aims to assess its efficacy and safety.

Methods

A multicenter, open-label, randomized controlled trial was conducted on 300 patients with non-severe COVID-19, randomly assigned into two groups: 150 receiving standard care (control group) and 150 receiving additional SCGJT for 10 days (SCGJT group). Time to resolution of symptoms, symptom severity, disease progression, time to discharge, the National Early Warning Score 2 (NEWS2) score, usage of Western drugs, time to viral clearance, and safety outcomes were continuously monitored.

Results

The SCGJT group exhibited faster symptom resolution (median: 9 vs. 13 days) and improved symptom severity, including cough, fatigue, hypogeusia, muscle aches, nasal congestion, runny nose, and sore throat, compared to the control group. Although there was a lower rate of severe progression in the SCGJT group (0.7% vs. 4.7%), the difference was not statistically significant. The time to discharge was significantly shorter in the SCGJT group (median: 7 vs. 8 days). Changes in the NEWS2 score did not show significant differences between groups. SCGJT has been demonstrated to reduce the need for symptomatic relief medications and hasten SARS-CoV-2 viral clearance. No adverse events were reported, and routine tests showed no significant differences.

Conclusions

SCGJT is safe and has potential clinical efficacy in non-severe COVID-19 patients. However, data regarding preventing severe progression remains inconclusive. Further studies should be conducted in light of the current state of the COVID-19 pandemic.

## Linked entities

- **Diseases:** COVID-19 (MONDO:0100096)

## Full-text entities

- **Diseases:** fatigue (MESH:D005221), hypogeusia (MESH:D000370), sore throat (MESH:D010612), nasal congestion (MESH:D009668), runny nose (MESH:D000086722), muscle aches (MESH:D063806), cough (MESH:D003371), COVID-19 (MESH:D000086382)
- **Chemicals:** SCGJT (-)
- **Species:** Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049], Homo sapiens (human, species) [taxon 9606]

## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11246756/full.md

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Source: https://tomesphere.com/paper/PMC11246756