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| Sponsor: | Tel-Aviv Sourasky Medical Center |
|---|---|
| Collaborator: |
Tel Aviv Medical Center |
| Information provided by: | Tel-Aviv Sourasky Medical Center |
| ClinicalTrials.gov Identifier: | NCT00950339 |
Purpose
Current guidelines recommend the addition of proton pump inhibitors (PPI) to patients taking double anti-platelet therapy (Aspirin and Clopidogrel) to prevent upper GI bleeding1. Many post percutaneous coronary intervention (PCI) patients are treated with dual anti-platelet medications as well as PPI to prevent upper GI bleeding.
Recently, it was shown that PPI interact with the P450 system in the liver and reduce the platelet inhibitory effect of Clopidogrel2,3. Clopidogrel is activated by CYP2C19, which also metabolizes PPI4. Furthermore, a recent article showed increased mortality in patients taking PPI and clopidogrel compared with patients taking clopidogrel without PPI protection5. The degree of reduction in the platelet inhibitory properties of clopidogrel might vary among the different PPI4.
The use of PPI for GI protection in patients treated with dual anti-platelet therapy is not based on randomized trials, but rather on expert opinion. Since H2 blockers are also effective in preventing acid secretion and are not known to interact with the P450 system that affects clopidogrel, the investigators hypothesized that these group of drugs will not interfere with the positive antiplatelet effects of clopidogrel and therefore will offer a good alternative treatment option.
| Condition | Intervention | Phase |
|---|---|---|
|
Coronary Heart Disease GI Bleeding |
Drug: PPI Platelet Inhibitory |
Phase IV |
| Study Type: | Interventional |
| Study Design: | Treatment, Non-Randomized, Open Label, Uncontrolled, Crossover Assignment, Pharmacokinetics/Dynamics Study |
| Official Title: | Platelet Inhibitory Effect of Clopidogrel in Patients Treated With Omeprazole, Pantoprazole, or Famotidine |
| Estimated Enrollment: | 50 |
| Study Start Date: | September 2009 |
| Estimated Study Completion Date: | December 2011 |
| Estimated Primary Completion Date: | December 2010 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
PPI Platelet Inhibitory: Experimental
Each patient will undergo 3 phases of drug therapy: A- 4 weeks of PPI treatment (omeprazole, 20mg twice daily)) B- 4 weeks of H2 blocker treatment (famotidine 40mg twice daily) C- 4 weeks of PPI treatment (pantoprazole 40mg once daily). At the end of each phase- each patient will undergo the following evaluation: Platelet reactivity |
Drug: PPI Platelet Inhibitory
Each patient will undergo 3 phases of drug therapy: A- 4 weeks of PPI treatment (omeprazole, 20mg twice daily)) B- 4 weeks of H2 blocker treatment (famotidine 40mg twice daily) C- 4 weeks of PPI treatment (pantoprazole 40mg once daily). At the end of each phase- each patient will undergo the following evaluation: Platelet reactivity |
In this study we will compare 3 different anti-acids regimens and their effect on platelet function
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
Contacts and Locations
More Information
| Responsible Party: | Tel Aviv medical center ( Prof. Shmuel Banai ) |
| Study ID Numbers: | TASMC-09-SB-0196-09-TLV-CTIL |
| Study First Received: | April 19, 2009 |
| Last Updated: | July 30, 2009 |
| ClinicalTrials.gov Identifier: | NCT00950339 History of Changes |
| Health Authority: | Israel: Ethics Commission |
|
GI bleeding clopidogrel aspirin prevention angiography |
|
Neurotransmitter Agents Molecular Mechanisms of Pharmacological Action Gastrointestinal Diseases Myocardial Ischemia Pantoprazole Hematologic Agents Physiological Effects of Drugs Omeprazole Arteriosclerosis Hemorrhage Pathologic Processes Famotidine Therapeutic Uses Anti-Ulcer Agents Cardiovascular Diseases |
Arterial Occlusive Diseases Heart Diseases Vascular Diseases Gastrointestinal Hemorrhage Gastrointestinal Agents Histamine Agents Enzyme Inhibitors Pharmacologic Actions Histamine H2 Antagonists Coronary Disease Digestive System Diseases Histamine Antagonists Clopidogrel Platelet Aggregation Inhibitors Coronary Artery Disease |