# Quzhuo tongbi formula for reducing gout flare related to uric acid lowering treatment: Study protocol for a multiple-center, randomized, double-blind, placebo, parallel-controlled clinical trial

**Authors:** Hejing Pan, Xuanlin Li, Shan Wu, Donghai Zhou, Haojie Guan, Haoyu Wu, Qiao Wang, Yujun Tang, Xuanming Hu, Meijiao Wang, Mingqian Zhou, Runyue Huang, Lei Liu, Yaolong Chen, Chengping Wen, Lin Huang

PMC · DOI: 10.1371/journal.pone.0327864 · 2025-07-09

## TL;DR

This study tests a traditional Chinese formula to reduce gout flare-ups during uric acid-lowering treatment in a clinical trial.

## Contribution

The study introduces a clinical trial protocol to evaluate the Qu-zhuo Tong-bi formula's effectiveness in preventing gout flares during urate-lowering therapy.

## Key findings

- The trial will assess gout flare frequency as the primary outcome.
- Secondary outcomes include flare duration, pain levels, and uric acid target achievement rates.

## Abstract

Gout, a prevalent metabolic rheumatic disease, arises from the accumulation of monosodium urate (MSU) crystals in joints, directly associated with hyperuricemia. Long-term or lifelong urate-lowering therapy (ULT) stands as the primary management strategy. However, there is a significant risk of gout flares during ULT, and current methods have drawbacks, including side effects. Previous research has suggested a potential benefit of the Qu-zhuo Tong-bi formula (QTF) in the treatment and prevention of gout. This study aims to evaluate the effectiveness and safety of QTF in reducing gout flares during ULT.

This is a multi-center, randomized, double-blind, placebo, parallel-controlled clinical trial conducted in four hospitals in Zhejiang Province, China. A total of 144 patients, aged 18–80 years, will be randomly allocated to either the intervention group (QTF + febuxostat) or the control group (placebo + febuxostat) for a 12-week treatment period. The primary outcome measure is the frequency of gout flares. Secondary outcome measures include the time from the patient’s enrollment to the first occurrence of gout flare (in days), duration of gout flare (in days), health assessment questionnaire disability index (HAQ-DI), pain level (visual analog scale – VAS), rate of achieving target uric acid levels. Occurrences of adverse events, and results from electrocardiograms and laboratory tests, will be monitored.

The findings from this study will offer valuable evidence supporting the efficacy of the QTF in reducing gout flares during ULT.

ChiCTR20084417 Register on May 16, 2024.

## Linked entities

- **Diseases:** gout (MONDO:0005393)

## Full-text entities

- **Diseases:** Gout (MESH:D006073), pain (MESH:D010146), hyperuricemia (MESH:D033461), rheumatic disease (MESH:D012216)
- **Chemicals:** Quzhuo tongbi (-), MSU (MESH:D014527)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12240339/full.md

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Source: https://tomesphere.com/paper/PMC12240339