Evidence map›Paper›PMID 40632763›Full record

ArticlePloS one2025

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.

Hejing Pan, Xuanlin Li, Shan Wu, Donghai Zhou, Haojie Guan, Haoyu Wu, Qiao Wang, Yujun Tang, Xuanming Hu, Meijiao Wang and 6 more

Erratum issuedAbstract readClinical Trial Protocol
In one paragraph

Article in PloS one, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors.

Hejing PanCollege of Basic Medical Science, Zhejiang Chinese Medical University, Hangzhou, China.
Xuanlin LiCollege of Basic Medical Science, Zhejiang Chinese Medical University, Hangzhou, China.
Shan Wuthe First Affiliated Hospital of Zhejiang Chinese Medical University, Hangzhou, China.
Donghai Zhouthe Second Affiliated Hospital of Zhejiang Chinese Medical University, Hangzhou, China.
Haojie GuanShengzhou People's Hospital, Shengzhou, China.
Haoyu WuHuzhou Hospital of Traditional Chinese Medicine, Huzhou, China.
Qiao WangCollege of Basic Medical Science, Zhejiang Chinese Medical University, Hangzhou, China.
Yujun TangCollege of Basic Medical Science, Zhejiang Chinese Medical University, Hangzhou, China.
Xuanming HuCollege of Basic Medical Science, Zhejiang Chinese Medical University, Hangzhou, China.
Meijiao WangCollege of Basic Medical Science, Zhejiang Chinese Medical University, Hangzhou, China.
Mingqian ZhouCollege of Basic Medical Science, Zhejiang Chinese Medical University, Hangzhou, China.
Runyue Huangthe Second Affiliated Hospital of Guangzhou University of Chinese Medicine.
Lei LiuDepartment of Rheumatology and Immunology, the Second Affiliated Hospital of Zhejiang University, Hangzhou, China.
Yaolong ChenCenter for Evidence-Based Medicine, Lanzhou University, Lanzhou, China.
Chengping WenCollege of Basic Medical Science, Zhejiang Chinese Medical University, Hangzhou, China.
Lin HuangCollege of Basic Medical Science, Zhejiang Chinese Medical University, Hangzhou, China.ORCID https://orcid.org/0000-0002-8036-8408

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionGout, 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.

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

trial registrationChiCTR20084417 Register on May 16, 2024.

Indexed as

Drugs, Chinese HerbalGoutGout SuppressantsUric AcidAdolescentAdultAgedAged, 80 and overChinaDouble-Blind MethodFebuxostatFemaleHumansHyperuricemiaMaleMiddle AgedDrugs, Chinese HerbalFebuxostatGout SuppressantsUric Acid

Identifiers

PMID40632763
PMCPMC12240339

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.