search
Back to results

Comparison of Two Dual Therapies in the First-line Treatment of Helicobacter Pylori Infection (SHARE2301)

Primary Purpose

Helicobacter Pylori Infection

Status
Recruiting
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
Tegoprazan
Amoxicillin
Esomeprazole
Sponsored by
Yanqing Li
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Helicobacter Pylori Infection

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Helicobacter pylori infection (either positive for histopathological test, rapid urease test, or C13/C14 urea breath test). Patients who have not previously received helicobacter pylori eradication therapy. Exclusion Criteria: Serious underlying diseases, such as liver insufficiency, renal insufficiency, immunosuppression, malignant tumor, coronary heart disease (angina pectoris or coronary artery stenosis ≥ 75%). 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.

Sites / Locations

  • Department of Gastroenterology, Qilu Hospital, Shandong UniversityRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

14-day Tegoprazan-Amoxicillin dual therapy

14-day Esomeprazole-Amoxicillin dual therapy

Arm Description

14-day Tegoprazan-Amoxicillin dual therapy, Tegoprazan(Luo Xin Pharmaceutical Group Co. LTD)50mg bid, Amoxicillin (Amoxicillin, United Laboratories Co. LTD) 750mg qid

14-day Esomeprazole-Amoxicillin dual therapy, Esomeprazole(Astrazeneca Pharmaceutical Co., LTD.) 20mg qid, Amoxicillin (Amoxicillin, United Laboratories Co. LTD) 750mg qid

Outcomes

Primary Outcome Measures

Eradication rate
Both intention to treat (ITT) and per-protocol (PP) analyses will be used for the assessment of the eradication rates of Helicobacter pylori infections in two groups. The ITT analysis includes all randomly assigned patients who take at least one dose of the study medications. The PP analysis is limited to patients who take over 80% of the study medications and complete follow-up.

Secondary Outcome Measures

Rate of adverse reactions
Rate of adverse reactions
Patient compliance
good compliance is defined as the actual dosage is within the range of 80%-100% of the dosage that should be taken

Full Information

First Posted
May 7, 2023
Last Updated
July 7, 2023
Sponsor
Yanqing Li
Collaborators
Linyi People's Hospital, Weifang Medical University, Zhengzhou Central Hospital, Yuncheng Traditional Chinese Medicine Hospital, The Affiliated Hospital of Qingdao University, The People's Hospital of Jimo, The Second Affiliated Hospital of Shandong University of traditional Chinese Medicine
search

1. Study Identification

Unique Protocol Identification Number
NCT05870683
Brief Title
Comparison of Two Dual Therapies in the First-line Treatment of Helicobacter Pylori Infection (SHARE2301)
Official Title
Comparison of the Efficacy of Tegoprazan-containing Versus Esomeprazole-containing Dual Therapy for Helicobacter Pylori Eradication: a Prospective, Multicenter, Randomized Controlled Study (SHARE2301)
Study Type
Interventional

2. Study Status

Record Verification Date
July 2023
Overall Recruitment Status
Recruiting
Study Start Date
May 24, 2023 (Actual)
Primary Completion Date
October 1, 2023 (Anticipated)
Study Completion Date
December 30, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Yanqing Li
Collaborators
Linyi People's Hospital, Weifang Medical University, Zhengzhou Central Hospital, Yuncheng Traditional Chinese Medicine Hospital, The Affiliated Hospital of Qingdao University, The People's Hospital of Jimo, The Second Affiliated Hospital of Shandong University of traditional Chinese Medicine

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
Helicobacter pylori (H. pylori) infection is a common global infectious disease of the gastrointestinal tract. Helicobacter pylori eradication can effectively prevent the development of stomach cancer. Progressive application of dual therapy for the eradication of Helicobacter pylori. Tegoprazan, a Potassium-Competitive Acid Blockers. The efficacy of P-CAB agents represented by vonoprazan in H. pylori eradication therapy has been widely verified.
Detailed Description
In 1989, it was suggested that amoxicillin combined with PPI could eradicate Hp infection, and in 2015, a prospective, multicenter, randomized controlled study in Taiwan with a large sample showed that the eradication rate of Hp could reach 96.6% with dual therapy for primary treatment of Hp infection, and the results of intention-to-treat analysis were as high as 95.3%. 95.3%. In 2020, a meta-analysis showed that high-dose dual therapy had the same efficacy and fewer side effects than other recommended regimens in first-line treatment. In terms of dosing days, multiple randomized controlled studies and meta-analyses from 2020-2021 have shown that 14 days of high-dose dual therapy is more effective in eradicating H. pylori. 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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Helicobacter Pylori Infection

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
368 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
14-day Tegoprazan-Amoxicillin dual therapy
Arm Type
Experimental
Arm Description
14-day Tegoprazan-Amoxicillin dual therapy, Tegoprazan(Luo Xin Pharmaceutical Group Co. LTD)50mg bid, Amoxicillin (Amoxicillin, United Laboratories Co. LTD) 750mg qid
Arm Title
14-day Esomeprazole-Amoxicillin dual therapy
Arm Type
Active Comparator
Arm Description
14-day Esomeprazole-Amoxicillin dual therapy, Esomeprazole(Astrazeneca Pharmaceutical Co., LTD.) 20mg qid, Amoxicillin (Amoxicillin, United Laboratories Co. LTD) 750mg qid
Intervention Type
Drug
Intervention Name(s)
Tegoprazan
Intervention Description
Included in dual eradication medication.
Intervention Type
Drug
Intervention Name(s)
Amoxicillin
Intervention Description
Included in dual eradication medication.
Intervention Type
Drug
Intervention Name(s)
Esomeprazole
Intervention Description
Included in dual eradication medication.
Primary Outcome Measure Information:
Title
Eradication rate
Description
Both intention to treat (ITT) and per-protocol (PP) analyses will be used for the assessment of the eradication rates of Helicobacter pylori infections in two groups. The ITT analysis includes all randomly assigned patients who take at least one dose of the study medications. The PP analysis is limited to patients who take over 80% of the study medications and complete follow-up.
Time Frame
Immediately after follow-up check
Secondary Outcome Measure Information:
Title
Rate of adverse reactions
Description
Rate of adverse reactions
Time Frame
Immediately after follow-up check
Title
Patient compliance
Description
good compliance is defined as the actual dosage is within the range of 80%-100% of the dosage that should be taken
Time Frame
Immediately after follow-up check

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Helicobacter pylori infection (either positive for histopathological test, rapid urease test, or C13/C14 urea breath test). Patients who have not previously received helicobacter pylori eradication therapy. Exclusion Criteria: Serious underlying diseases, such as liver insufficiency, renal insufficiency, immunosuppression, malignant tumor, coronary heart disease (angina pectoris or coronary artery stenosis ≥ 75%). 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.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Yanqing Li, MD
Phone
18560086667
Email
qlxhkqz@163.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Yanqing Li
Organizational Affiliation
Qilu Hospital of Shandong University
Official's Role
Study Chair
Facility Information:
Facility Name
Department of Gastroenterology, Qilu Hospital, Shandong University
City
Jinan
State/Province
Shandong
ZIP/Postal Code
250012
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Yanqing Li, PhD. MD.
Phone
18678827666
Email
liyanqing@sdu.edu.cn

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
27707777
Citation
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.
Results Reference
result

Learn more about this trial

Comparison of Two Dual Therapies in the First-line Treatment of Helicobacter Pylori Infection (SHARE2301)

We'll reach out to this number within 24 hrs