Evidence map›Paper›PMID 40151129›Full record

ArticleJournal of traditional Chinese medicine = Chung i tsa chih ying wen pan2025

Efficacy and safety of Qingwei Zhitong pellets-containing quadruple therapy for eradication: a prospective, single-center, randomized trial.

Cheng Jianping, Fan Chanjuan, Zhai Lili, Wang Hui, Xie Dongling, Cai Yong, L I Zhen, Huang Kun, Bai Qixuan

Abstract readEquivalence Trial
In one paragraph

Article in Journal of traditional Chinese medicine = Chung i tsa chih ying wen pan, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Cheng JianpingDepartment of Gastroenterology and Oncology, Civil Aviation General Hospital, Beijing 100123, China.
Fan ChanjuanDepartment of Gastroenterology and Oncology, Civil Aviation General Hospital, Beijing 100123, China.
Zhai LiliDepartment of Gastroenterology and Oncology, Civil Aviation General Hospital, Beijing 100123, China.
Wang HuiDepartment of Gastroenterology and Oncology, Civil Aviation General Hospital, Beijing 100123, China.
Xie DonglingDepartment of Gastroenterology and Oncology, Civil Aviation General Hospital, Beijing 100123, China.
Cai YongDepartment of Gastroenterology and Oncology, Civil Aviation General Hospital, Beijing 100123, China.
L I ZhenDepartment of Gastroenterology and Oncology, Civil Aviation General Hospital, Beijing 100123, China.
Huang KunDepartment of Gastroenterology and Oncology, Civil Aviation General Hospital, Beijing 100123, China.
Bai QixuanDepartment of Gastroenterology and Oncology, Civil Aviation General Hospital, Beijing 100123, China.

Funding

China Zhongguancun Precision Medicine Science and Technology Foundation: Study on the Evaluation of Eradication Rate and Safety of Helicobacter Pylori in a Quadruple Therapy using Qingwei Zhitong Pellets as a Substitute for Bismuth Agent 320.6799.2022.09.24
6 · The paper itself

Abstract

objectiveTo evaluate the efficacy and safety of 14-day Qingwei Zhitong pellets (, QZ)-containing quadruple therapy (QZQT) compared to bismuth-containing quadruple therapy (BQT) in treatment-naive patients with

methodsThis single-center, randomized controlled clinical trial enrolled 333 patients, who were divided into either the QZQT group (QZ pellets, 3.2 g, three times daily; rabeprazole, 10 mg, twice daily; amoxicillin 1000 mg, twice daily; clarithromycin, 500 mg, twice daily) or the BQT group (bismuth potassium citrate, 1000 mg, three times daily; rabeprazole, 10 mg, twice daily; amoxicillin, 1000 mg, twice daily; clarithromycin, 500 mg, twice daily) for 14 d. The 13C-urea breath test assessed eradication success at least four weeks after treatment. The primary outcome focused on the eradication rate, with secondary outcomes including safety and patient compliance.

resultsFrom August 2022 to June 2023, 342 subjects were screened, and 333 were randomized. The QZQT and BQT groups showed eradication rates of 68.9% and 67.8% (

conclusionThe 14 d QZQT treatment demonstrates equal efficacy in eradicating H. pylori infection and improved patient compliance and safety compared to BQT. These results provide evidence supporting 14-day QZQT as an acceptable treatment for

Indexed as

Anti-Bacterial AgentsDrugs, Chinese HerbalHelicobacter InfectionsAdultAgedAmoxicillinClarithromycinDrug Therapy, CombinationFemaleHelicobacter pyloriHumansMaleMiddle AgedProspective StudiesTreatment OutcomeYoung AdultAmoxicillinAnti-Bacterial AgentsClarithromycinDrugs, Chinese HerbalbismutheradicationQingwei Zhitong pelletsquadruple therapyrandomized controlled trial

Identifiers

PMID40151129
PMCPMC11955757

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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.