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
| Type | Name | Description |
|---|---|---|
| DRUG | histamine-2 receptor antagonist | famotidine 40 mg qd plus thienopyridine |
| DRUG | Placebo | placebo 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.