|
Home
Search
Study Topics
Glossary
|
![]() |
![]() |
|
![]() |
|
![]() |
|
![]() |
![]() |
![]() |
|
![]() |
![]() |
||||||||||||||||||||||||||||||||||||
| Sponsor: | Deutsches Herzzentrum Muenchen |
|---|---|
| Information provided by (Responsible Party): | Deutsches Herzzentrum Muenchen |
| ClinicalTrials.gov Identifier: | NCT01339819 |
Purpose
The aim of this study is to evaluate whether Dabigatran itself reduces ADP induced platelet aggregation measured by MEA as compared to Phenprocoumon after a two-week treatment with either agent.
| Condition | Intervention | Phase |
|---|---|---|
|
Atrial Fibrillation |
Drug: Dabigatran Drug: Phenprocoumon |
Phase 4 |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Pharmacokinetics/Dynamics Study Intervention Model: Parallel Assignment Masking: Open Label Primary Purpose: Treatment |
| Official Title: | Impact of Dabigatran and Phenprocoumon on ADP Induced Platelet Aggregation in Patients With Atrial Fibrillation |
| Estimated Enrollment: | 70 |
| Study Start Date: | April 2011 |
| Estimated Study Completion Date: | June 2012 |
| Estimated Primary Completion Date: | May 2012 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Experimental: Arm 1
Dabigatran Therapy
|
Drug: Dabigatran
Patients assigned to this group will receive Dabigatran
Other Name: Pradaxa
|
|
Active Comparator: Arm 2
Phenprocoumon Therapy
|
Drug: Phenprocoumon
Patients assigned to this group will receive Phenprocoumon
Other Name: Marcumar
|
Oral anticoagulation with vitamin K antagonists (OAC) is the standard care for reducing stroke in patients with atrial fibrillation. Just recently the direct, competitive thrombin inhibitor dabigatran has been approved by the FDA for stroke prevention in patients with atrial fibrillation. In a large multicenter trial it was shown that dabigatran was at least as effective as Vitamin K antagonists in the prevention of stroke without an increase of major hemorrhage.
Approximately 6 % of patients who undergo coronary stenting and need DAT with aspirin and clopidogrel need in addition OAC for the reduction of cardiac, cerebral and systemic thromboembolic events. These patients will therefore need triple therapy, a therapy which is associated with increased bleeding complications. Although phenprocoumon given solely without clopidogrel has no impact on ADP induced platelet aggregation, it has been shown that phenprocoumon significantly attenuates the antiplatelet effects of clopidogrel.
ADP induced platelet aggregation measured with multiple electrode platelet aggregometry (MEA) is a marker for the efficacy of the clopidogrel therapy and (i) a low response (AUC ≥ 468) to clopidogrel has been associated with an increase of ischemic events such as stent thrombosis and (ii) patients with an enhanced response to clopidogrel (AUC ≤ 188) have higher bleeding rates.
It is therefore crucial to evaluate whether an additional antithrombotic therapy such as dabigatran alters ADP induced platelet aggregation in these patients. While it has been shown that intravenous administration of the direct thrombin inhibitor bivalirudin further reduces ADP induced platelet aggregation in patients on clopidogrel therapy, it is unknown whether dabigatran has also an impact on ADP induced platelet aggregation.
To evaluate the impact of dabigatran on ADP induced platelet aggregation we will randomize patients with atrial fibrillation and the need for oral anticoagulation for a two-week treatment with either dabigatran or phenprocoumon and we hypothesize that dabigatran is superior to phenprocoumon in the reduction of ADP induced platelet aggregation. Patients who are concomitantly treated with clopidogrel are being studied in a different trial with a similar study design (Dabi ADP-2).
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Key Inclusion Criteria:
Key Exclusion Criteria:
Contacts and Locations| Contact: Julinda Mehilli, MD | +49 89 1218-4582 | Mehilli@dhm.mhn.de |
| Contact: Nikolaus Sarafoff, MD | +49 89 1218-4073 | n.sarafoff@googlemail.com |
| Germany | |
| Deutsches Herzzentrum Muenchen | Recruiting |
| Munich, Germany, 80636 | |
| Contact: Julinda Mehilli, MD +49 89 1218-4582 Mehilli@dhm.mhn.de | |
| Contact: Nikolaus Sarafoff, MD +49 89 1218-4073 n.sarafoff@googlemail.com | |
| Principal Investigator: | Julinda Mehilli, MD | Deutsches Herzzentrum München, Klinik für Herz- und Kreislauferkrankungen |
More Information
| Responsible Party: | Deutsches Herzzentrum Muenchen |
| ClinicalTrials.gov Identifier: | NCT01339819 History of Changes |
| Other Study ID Numbers: | GE IDE No. A01611, 2011-000503-40 |
| Study First Received: | April 15, 2011 |
| Last Updated: | April 24, 2012 |
| Health Authority: | Germany: Federal Institute for Drugs and Medical Devices |
|
Atrial Fibrillation Arrhythmias, Cardiac Heart Diseases Cardiovascular Diseases Pathologic Processes |
Phenprocoumon Anticoagulants Hematologic Agents Therapeutic Uses Pharmacologic Actions |