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

Primary Purpose

Peptic Ulcer

Status
Completed
Phase
Not Applicable
Locations
Taiwan
Study Type
Interventional
Intervention
histamine-2 receptor antagonist
Placebo
Sponsored by
Kaohsiung Veterans General Hospital.
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Peptic Ulcer focused on measuring histamine-2 receptor antagonist, peptic ulcer, thienopyridine, prevention

Eligibility Criteria

20 Years - 90 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. The past history of gastroduodenal ulcer and underwent endoscopy for dyspeptic symptoms.
  2. thienopyridine users without baseline gastroduodenal ulcer at initial endoscopy.
  3. They are adult patients aged least 20 years of age.

Exclusion Criteria:

  1. They have a history of gastric or duodenal surgery other than oversewing of a perforation.
  2. They require long-term treatment with non-steroidal anti-inflammatory drugs.
  3. serious disease.

Sites / Locations

  • Kaohsiung Veterans General Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

histamine-2 receptor antagonist group

placebo group

Arm Description

famotidine 40mg qd for 6 months.

placebo for 6 months.

Outcomes

Primary Outcome Measures

Number of Participants With Healed Peptic Ulcer
Follow-up endoscopy was performed at the end of the 6th month

Secondary Outcome Measures

Full Information

First Posted
April 12, 2015
Last Updated
March 8, 2019
Sponsor
Kaohsiung Veterans General Hospital.
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1. Study Identification

Unique Protocol Identification Number
NCT02418312
Brief Title
Efficacy of H2 Receptor Antagonist in Prevention of Thienopyridine-related Peptic Ulcer
Official Title
Efficacy of H2 Receptor Antagonist in Prevention of Thienopyridine-related Peptic Ulcer
Study Type
Interventional

2. Study Status

Record Verification Date
March 2019
Overall Recruitment Status
Completed
Study Start Date
January 2012 (undefined)
Primary Completion Date
October 2017 (Actual)
Study Completion Date
October 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Kaohsiung Veterans General Hospital.

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief 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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Peptic Ulcer
Keywords
histamine-2 receptor antagonist, peptic ulcer, thienopyridine, prevention

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
228 (Actual)

8. Arms, Groups, and Interventions

Arm Title
histamine-2 receptor antagonist group
Arm Type
Active Comparator
Arm Description
famotidine 40mg qd for 6 months.
Arm Title
placebo group
Arm Type
Placebo Comparator
Arm Description
placebo for 6 months.
Intervention Type
Drug
Intervention Name(s)
histamine-2 receptor antagonist
Other Intervention Name(s)
famotidine 40 mg qd
Intervention Description
famotidine 40 mg qd plus thienopyridine
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
placebo plus thienopyridine
Primary Outcome Measure Information:
Title
Number of Participants With Healed Peptic Ulcer
Description
Follow-up endoscopy was performed at the end of the 6th month
Time Frame
6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
90 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: The past history of gastroduodenal ulcer and underwent endoscopy for dyspeptic symptoms. thienopyridine users without baseline gastroduodenal ulcer at initial endoscopy. They are adult patients aged least 20 years of age. Exclusion Criteria: They have a history of gastric or duodenal surgery other than oversewing of a perforation. They require long-term treatment with non-steroidal anti-inflammatory drugs. serious disease.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ping-I Hsu, Bachelor
Organizational Affiliation
Kaohsiung Veterans General Hospital.
Official's Role
Study Chair
Facility Information:
Facility Name
Kaohsiung Veterans General Hospital
City
Kaohsiung
ZIP/Postal Code
813
Country
Taiwan

12. IPD Sharing Statement

Plan to Share IPD
No
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Efficacy of H2 Receptor Antagonist in Prevention of Thienopyridine-related Peptic Ulcer

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