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Triple Therapy in Patients on Oral Anticoagulation After Drug Eluting Stent Implantation

Intracoronary Stenting and Antithrombotic Regimen: Testing of a Six-week Versus a Six-month Clopidogrel Treatment Regimen in Patients With Concomitant Aspirin and Oral Anticoagulant Therapy Following Drug-eluting Stenting

Status
UNKNOWN
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00776633
Acronym
ISAR-TRIPLE
Enrollment
614
Registered
2008-10-21
Start date
2008-09-30
Completion date
2014-09-30
Last updated
2016-08-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Atrial Fibrillation, Coronary Artery Disease

Keywords

aspirin, clopidogrel, oral anticoagulation, warfarin, drug eluting stent, phenprocoumon

Brief summary

The investigators hypothesize that reducing the duration of clopidogrel therapy from 6 months to 6 weeks after DES implantation is associated with improved clinical outcomes in patients on ASA and an oral anticoagulant.

Detailed description

The introduction of drug-eluting stents (DES) was associated not only with a widening of the indication for percutaneous coronary intervention (PCI) but also with longer antithrombotic therapy duration. Dual antiplatelet therapy with ASA and a thienopyridine is very efficient in preventing adverse events after coronary stenting but it is inferior to oral anticoagulation (OAC) to reduce the risk of stroke in patients with atrial fibrillation. OAC is also superior to antiplatelet therapy in patients with mechanical heart valves and the therapy of choice for the treatment of deep vein thrombosis and pulmonary embolism. OAC is also administered for left ventricular thrombi and low ejection fraction. There is an increasing number of patients undergoing coronary stenting who are in need of life-long anticoagulation therapy and would therefore require a triple therapy consisting of aspirin, clopidogrel and oral anticoagulation. As oral anticoagulation and antithrombotic therapy impair primary and secondary hemostasis there are concerns that adding warfarin to dual antiplatelet therapy might cause increased bleeding rates. Several studies have retrospectively assessed efficacy and safety in patients receiving a triple therapy with various results: major bleeding rates varied from 3,1%-14,9% with total bleeding rates up to 27,5%. Prospective randomized data on this topic are not available. Therefore the aim of this study is to compare a 6 week versus a 6 month triple therapy after DES implantation.

Interventions

DRUGaspirin

6 weeks triple therapy with aspirin, clopidogrel and oral anticoagulation

DRUGclopidogrel

6 months triple therapy with aspirin, clopidogrel and oral anticoagulation

DRUGoral anticoagulation

Sponsors

Deutsches Herzzentrum Muenchen
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Key Inclusion Criteria: 1. Patients with an indication for oral anticoagulation and a DES implantation. 2. Informed, written consent by the patient or her/his legally-authorized representative for participation in the study. Key

Exclusion criteria

1. Age ≤18 years 2. Previous stent thrombosis 3. DES in left main

Design outcomes

Primary

MeasureTime frame
Composite of death, myocardial infarction, definite stent thrombosis, stroke or major bleeding.9 months

Secondary

MeasureTime frame
Ischemic complications (composite of cardiac death, myocardial infarction, stent thrombosis or ischemic stroke)9 months
Bleeding complications (Major bleeding)9 months

Countries

Denmark, Germany

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 17, 2026