Trials / Completed
CompletedNCT01896557
Ranitidin Versus Omeprazole in Patients Taking Clopidogrel
Possible Drug Interaction Between Clopidogrel and Ranitidin or Omeprazole in Patients With Stable Coronary Heart Disease: a Comparative Study
- Status
- Completed
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 92 (actual)
- Sponsor
- University of Sao Paulo General Hospital · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
Previous reports have shown a possible drug interaction between clopidogrel and proton pump inhibitors (PPI´s), which could result in increased number of adverse cardiovascular events among patients on dual antiplatelet therapy(DAPT). Because of this, ranitidin has been proposed as an alternative drug to PPI´s for prophylaxis of gastrointestinal bleeding in patients who need DAPT. The study´s aim is to test the hypothesis that ranitidin doesn´t have any influence on clopidogrel pharmacodynamic.
Detailed description
Study population: 100 patients with Stable Coronary Artery Disease from Heart Institute Inclusion Criteria: * Age \> 18 years old * Coronary artery disease, defined as previous myocardial infarction and/or coronary angioplasty and/or Coronary Artery Bypass Graft (CABG) surgery and/or coronariography showing obstruction of at least 50 % in one of major epicardial vessels * Treatment with Acetylsalicylic Acid (ASA) 100 mg/day Exclusion Criteria: * Use in the last 7 days of oral anticoagulant or any other antiplatelet drug beside ASA * Previous utilization of PPI or ranitidine in the last 7 days before randomization * Active bleeding * Pregnancy or woman of childbearing age without contraceptive method * Hemoglobin \< 10 g/dL or hematocrit \< 30 %, hematocrit \> 50 %, platelets \< 100.000/mm3 or \> 500.000/mm3; creatinin clearance \< 50 ml/minute * Percutaneous coronary intervention (PCI) on the last 30 days before randomization (or PCI on the last year when drug-eluted stents are used); CABG surgery on the last 90 days; acute coronary syndrome on the last 60 days * Active malignant neoplasm * Active peptic ulcer disease on the last 60 days or upper gastrointestinal bleeding any time in life * Known allergy to the drugs clopidogrel, ranitidine or omeprazole * Refuse to participate in the study\] Methodology: The study has a double-blind, double-dummy prospective design. Clopidogrel action is evaluated by platelet function tests: VerifyNow, bioimpedance aggregometry and Platelet Function Analyzer-100 (PFA-100). The patients have measurements of platelet function on three moments: before starting clopidogrel; 1 week after DAPT with clopidogrel (without loading dose) plus ASA; and after 1 week of randomization to ranitidin 150 mg bid or omeprazole 20 mg bid.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | omeprazole | Influence of omeprazole on clopidogrel pharmacodynamics will be evaluated. |
| DRUG | Ranitidine | Influence of ranitidine on clopidogrel pharmacodynamics will be evaluated. |
| DRUG | Clopidogrel | Clopidogrel added to ASA therapy at the first medical visit, Open label 75 mg once a day will be given to all individuals as part of the protocol (since main outcome of interest is clopidogrel effect. Actual comparison arms are double blind ranitidine and omeprazole |
Timeline
- Start date
- 2011-10-01
- Primary completion
- 2013-06-01
- Completion
- 2013-06-01
- First posted
- 2013-07-11
- Last updated
- 2018-07-06
- Results posted
- 2016-05-23
Source: ClinicalTrials.gov record NCT01896557. Inclusion in this directory is not an endorsement.