Clinical Trials Directory

Trials / Completed

CompletedNCT02418312

Efficacy of H2 Receptor Antagonist in Prevention of Thienopyridine-related Peptic Ulcer

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
228 (actual)
Sponsor
Kaohsiung Veterans General Hospital. · Academic / Other
Sex
All
Age
20 Years – 90 Years
Healthy volunteers
Not accepted

Summary

Whether H2 receptor antagonist can prevent thienopyridine-related peptic ulcer remains unclear.

Detailed description

The aim of the prospective, randomized study is investigate the efficacy of H2 receptor antagonist in prevention of thienopyridine-related peptic ulcer and gastrointestinal bleeding in patients with an ulcer history. We plan to enroll 236 thienopyridine (clopidogrel or ticlopidine) users with a peptic ulcer history who don't have baseline gastroduodenal ulcers at initial endoscopy . The patients will be randomly assigned to receive either (1) famotidine (40 mg qd) plus thienopyridine used previously or (2) placebo plus thienopyridine treatment alone for 6 months. The ulcer recurrence rate between the treatment gruops will be compared.

Conditions

Interventions

TypeNameDescription
DRUGhistamine-2 receptor antagonistfamotidine 40 mg qd plus thienopyridine
DRUGPlaceboplacebo plus thienopyridine

Timeline

Start date
2012-01-01
Primary completion
2017-10-01
Completion
2017-10-01
First posted
2015-04-16
Last updated
2019-03-11
Results posted
2019-03-11

Locations

1 site across 1 country: Taiwan

Source: ClinicalTrials.gov record NCT02418312. Inclusion in this directory is not an endorsement.