Evidence map›Paper›PMID 42622367›Full record

Trial reportHelicobacter

14-Day Vonoprazan-Minocycline Dual Therapy Versus Bismuth-Containing Quadruple Therapy for Helicobacter pylori Rescue Treatment: A Single-Center Randomized Controlled Noninferiority Trial.

Tingting Yang, Ruijuan Xin, Yanhong Deng, Jun Liu, Xue Li, Xiaole Guo, Linke Ma, Xiaoming Su, Yanxia Liu, Chengdong Su and 9 more

Abstract readRandomized Controlled TrialEquivalence Trial
In one paragraph

Trial report in Helicobacter. 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
–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

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

19 authors.

Tingting YangThe Third Clinical Medical College, Ningxia Medical University, Yinchuan, China.ORCID https://orcid.org/0009-0007-2078-8965
Ruijuan XinDepartment of Gastroenterology, People's Hospital of Ningxia Hui Autonomous Region, Affiliated People's Hospital of Ningxia Medical University, Yinchuan, China.
Yanhong DengDepartment of Gastroenterology, People's Hospital of Ningxia Hui Autonomous Region, Affiliated People's Hospital of Ningxia Medical University, Yinchuan, China.
Jun LiuDepartment of Gastroenterology, People's Hospital of Ningxia Hui Autonomous Region, Affiliated People's Hospital of Ningxia Medical University, Yinchuan, China.
Xue LiDepartment of Gastroenterology, People's Hospital of Ningxia Hui Autonomous Region, Affiliated People's Hospital of Ningxia Medical University, Yinchuan, China.
Xiaole GuoDepartment of Gastroenterology, People's Hospital of Ningxia Hui Autonomous Region, Affiliated People's Hospital of Ningxia Medical University, Yinchuan, China.ORCID https://orcid.org/0009-0009-2397-2930
Linke MaDepartment of Gastroenterology, People's Hospital of Ningxia Hui Autonomous Region, Affiliated People's Hospital of Ningxia Medical University, Yinchuan, China.
Xiaoming SuThe Third Clinical Medical College, Ningxia Medical University, Yinchuan, China.ORCID https://orcid.org/0000-0002-6676-8800
Yanxia LiuThe Third Clinical Medical College, Ningxia Medical University, Yinchuan, China.ORCID https://orcid.org/0009-0006-3237-7242
Chengdong SuDepartment of Gastroenterology, People's Hospital of Ningxia Hui Autonomous Region, Affiliated People's Hospital of Ningxia Medical University, Yinchuan, China.
Qian HaoDepartment of Gastroenterology, People's Hospital of Ningxia Hui Autonomous Region, Affiliated People's Hospital of Ningxia Medical University, Yinchuan, China.
Rui MuDepartment of Gastroenterology, People's Hospital of Ningxia Hui Autonomous Region, Affiliated People's Hospital of Ningxia Medical University, Yinchuan, China.
Xiaofei LiDepartment of Gastroenterology, People's Hospital of Ningxia Hui Autonomous Region, Affiliated People's Hospital of Ningxia Medical University, Yinchuan, China.
Pengda WangDepartment of Gastroenterology, People's Hospital of Ningxia Hui Autonomous Region, Affiliated People's Hospital of Ningxia Medical University, Yinchuan, China.
Yanling LiDepartment of Gastroenterology, People's Hospital of Ningxia Hui Autonomous Region, Affiliated People's Hospital of Ningxia Medical University, Yinchuan, China.
Xue ZhangThe Third Clinical Medical College, Ningxia Medical University, Yinchuan, China.
Qingrui LiThe Third Clinical Medical College, Ningxia Medical University, Yinchuan, China.
Yuting WuDepartment of Gastroenterology, People's Hospital of Ningxia Hui Autonomous Region, Affiliated People's Hospital of Ningxia Medical University, Yinchuan, China.
Shengjuan HuDepartment of Gastroenterology, People's Hospital of Ningxia Hui Autonomous Region, Affiliated People's Hospital of Ningxia Medical University, Yinchuan, China.ORCID https://orcid.org/0009-0000-2444-1992

Funding

Key Achievements in Science and Technology Transformation Project of Ningxia Hui Autonomous Region 2024CJE09045
6 · The paper itself

Abstract

backgroundRescue treatment for Helicobacter pylori infection remains challenging in regions with high antibiotic resistance. Although bismuth-containing quadruple therapy is widely recommended as an empirical rescue regimen, its medication burden may impair tolerability and adherence. This trial evaluated the efficacy and safety of 14-day vonoprazan-minocycline dual therapy compared with vonoprazan-based bismuth-containing quadruple therapy as empirical rescue treatment. MATERIALS AND

methodsThis single-center, prospective, open-label, randomized, controlled, noninferiority trial enrolled 186 adults aged 18-70 years with at least one previous H. pylori eradication failure. Patients were randomly assigned (1:1) to receive 14-day vonoprazan-minocycline dual therapy or vonoprazan-, amoxicillin-, minocycline-, and bismuth-containing quadruple therapy. Eradication was assessed by a

resultsEradication rates in the dual therapy and quadruple therapy groups were 89.2% and 91.4% in the ITT analysis (difference, -2.2%; 95% CI, -10.5% to 6.2%; noninferiority p = 0.036), 90.2% and 92.4% in the mITT analysis (difference, -2.2%; 95% CI, -9.7% to 5.3%; noninferiority p = 0.030), and 91.2% and 93.4% in the PP analysis (difference, -2.2%; 95% CI, -9.4% to 5.0%; noninferiority p = 0.024). Noninferiority was demonstrated in the mITT and PP analyses, whereas the ITT result should be interpreted cautiously because the lower 95% CI bound crossed the margin. Adverse events were similar between treatment groups (11.8% vs. 15.1%; χ

conclusions14-day vonoprazan-minocycline dual therapy achieved eradication rates comparable to those of bismuth-containing quadruple therapy, with acceptable safety and high adherence as rescue treatment for H. pylori infection. This simplified regimen may be considered a potential empirical rescue option when susceptibility testing is not readily available, although the ITT noninferiority result warrants cautious interpretation.

Indexed as

Anti-Bacterial AgentsBismuthHelicobacter InfectionsHelicobacter pyloriMinocyclinePyrrolesSulfonamidesAdolescentAdultAgedAmoxicillinDrug Therapy, CombinationFemaleHumansMaleMiddle AgedAmoxicillinAnti-Bacterial AgentsBismuthMinocyclinePyrrolesSulfonamidesvonoprazandual therapyHelicobacter pyloriminocyclinerescue treatmentvonoprazan

Identifiers

PMID42622367
PMCPMC13492090

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.