Comparison of Two Dual Therapies in the First-line Treatment of Helicobacter Pylori Infection (SHARE2301)
NCT ID: NCT05870683
Last Updated: 2023-07-11
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
NA
368 participants
INTERVENTIONAL
2023-05-24
2023-12-30
Brief Summary
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Detailed Description
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Tegoprazan, a Potassium-Competitive Acid Blockers (P-CAB), is a new type of acid-suppressing drug that compensates for the short half-life of acid-activated traditional acid-suppressing PPI and the low mucosal healing rate due to insufficient acid suppression. The efficacy of P-CAB agents represented by vonoprazan in H. pylori eradication therapy has been widely verified. 2022, tegoprazan was approved by the State Drug Administration for the new indication of eradication of H. pylori infection in adults in combination with appropriate antimicrobial therapy, and its efficacy in clinical application has not yet been verified.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
NONE
Study Groups
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14-day Tegoprazan-Amoxicillin dual therapy
14-day Tegoprazan-Amoxicillin dual therapy, Tegoprazan(Luo Xin Pharmaceutical Group Co. LTD)50mg bid, Amoxicillin (Amoxicillin, United Laboratories Co. LTD) 750mg qid
Tegoprazan
Included in dual eradication medication.
Amoxicillin
Included in dual eradication medication.
14-day Esomeprazole-Amoxicillin dual therapy
14-day Esomeprazole-Amoxicillin dual therapy, Esomeprazole(Astrazeneca Pharmaceutical Co., LTD.) 20mg qid, Amoxicillin (Amoxicillin, United Laboratories Co. LTD) 750mg qid
Amoxicillin
Included in dual eradication medication.
Esomeprazole
Included in dual eradication medication.
Interventions
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Tegoprazan
Included in dual eradication medication.
Amoxicillin
Included in dual eradication medication.
Esomeprazole
Included in dual eradication medication.
Eligibility Criteria
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Inclusion Criteria
* Patients who have not previously received helicobacter pylori eradication therapy.
Exclusion Criteria
* Those who are not willing to take contraceptive measures during pregnancy, lactation or the trial.
* Active gastrointestinal bleeding.
* History of drug allergy.
* History of upper gastrointestinal surgery.
* Medication history of bismuth, antibiotics and PPI within 4 weeks.
* Other behaviors that may increase the risk, such as alcohol and drug abuse.
* Unable or unwilling to provide informed consent.
18 Years
65 Years
ALL
No
Sponsors
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Linyi People's Hospital
OTHER
Weifang Medical University
OTHER
Zhengzhou Central Hospital
OTHER
Yuncheng Traditional Chinese Medicine Hospital
OTHER
The Affiliated Hospital of Qingdao University
OTHER
The People's Hospital of Jimo
UNKNOWN
Shandong University of Traditional Chinese Medicine
OTHER
Yanqing Li
OTHER
Responsible Party
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Yanqing Li
Vice-President
Principal Investigators
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Yanqing Li
Role: STUDY_CHAIR
Qilu Hospital of Shandong University
Locations
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Department of Gastroenterology, Qilu Hospital, Shandong University
Jinan, Shandong, China
Countries
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Central Contacts
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Facility Contacts
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References
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Malfertheiner P, Megraud F, O'Morain CA, Gisbert JP, Kuipers EJ, Axon AT, Bazzoli F, Gasbarrini A, Atherton J, Graham DY, Hunt R, Moayyedi P, Rokkas T, Rugge M, Selgrad M, Suerbaum S, Sugano K, El-Omar EM; European Helicobacter and Microbiota Study Group and Consensus panel. Management of Helicobacter pylori infection-the Maastricht V/Florence Consensus Report. Gut. 2017 Jan;66(1):6-30. doi: 10.1136/gutjnl-2016-312288. Epub 2016 Oct 5.
Kong Q, Mirza IA, Zhang X, Song X, Li X, Zhang Q, Xu L, Guo Y, Yu Y, Zuo X, Li Y, Li Y. Fourteen-Day Tegoprazan-Amoxicillin Dual Therapy as the First-Line Treatment of Helicobacter pylori Infection (SHARE2301): A Multicenter, Noninferiority, Randomized Clinical Trial. Helicobacter. 2024 May-Jun;29(3):e13098. doi: 10.1111/hel.13098.
Other Identifiers
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SHARE2301
Identifier Type: -
Identifier Source: org_study_id
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