CompletedInterventionalPhase 4Updated Dec 24, 2018
Modified Non-clarithromycin Triple Therapy in Eradicating Helicobacter Pylori
ClinicalTrials.gov ID
NCT02776371
Lead Sponsor
Shandong UniversityOTHER
Overall Status
Completed
Study Type
Interventional
Phase
Phase 4
Enrollment
301Actual
Last Update Posted
Dec 24, 2018Actual
Start Date
Sep 2016Actual
Primary Completion Date
Jan 2018Actual
Completion Date
Feb 2018Actual
Brief Summary
Helicobacter pylori (H. pylori) infects more than 50% of the population in the world(1), especially 47-66% in China.
Helicobacter Pylori Eradication Rate
Modified non-clarithromycin triple therapy
Sequential therapy
Ages Eligible for Study
Adult (18-64)Older Adult (65+)
Sexes Eligible for Study
All
Accepts Healthy Volunteers
Yes
Eligibility Criteria
Inclusion Criteria:
Patients who were intend to undergo upper endoscopy for any purpose and volunteered to written inform consent.
Exclusion Criteria:
negative in rapid urease test (RUT)
previous standard eradication therapy for H. pylori;
history of esophagectomy or gastrectomy;
gastrointestinal malignancy;
contraindications or allergic to study drugs;
user of taking medicine that may affect the result of the study within 4 weeks (e.g., proton-pump inhibitors, H2-receptor antagonists, bismuth or antibiotics etc.);
cardiopulmonary, hepatic or renal insufficiency, and/or severe current diseases or malignancy;
pregnant or lactating women;
participants of other trial within the past 3 months;
unwilling or unable to participate in the study.
Primary Purpose
Treatment
Allocation
Randomized
Interventional Model
Parallel Assignment
Masking
None (Open Label)
No central contacts
There are no central contacts for this study.
Department of Gastroenterology, Qilu Hospital, Shandong University