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Randomized, Double-Blind, Placebo-controlled Trial of 6 vs. 12 Months Clopidogrel Therapy After Implantation of a Drug-Eluting Stent
The purpose of this study is to determine whether a 6 month duration of clopidogrel therapy after DES implantation is not inferior to that of a 12 month therapy.
Drug elution from stent struts is associated with less smooth muscle cell proliferation and delayed stent strut re-endothelialization. Thus it seems conceivable that a longer duration of dual antiplatelet therapy (aspirin and clopidogrel) after DES implantation is needed. However, no studies have been done to investigate which is the optimal antiplatelet therapy duration after DES implantation. Therefore, the objective of the randomized, double-blind, placebo-controlled ISAR-SAFE study is to evaluate the safety and efficacy of a 6 month versus a 12 month duration of clopidogrel therapy after DES implantation. Patients on clopidogrel therapy at least 6 months after DES implantation, who do not require a reintervention will be randomized to an additional 6 month period of clopidogrel or placebo. The patients will be followed-up for 9 months after randomization.
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
No
University of Florida, Health Science Center - Jacksonville
Jacksonville, Florida, United States
Spitali Gjerman
Tirana, Albania
Krankenanstalt Rudolfstiftung
Vienna, Austria
Wilhelminenspital Wien
Vienna, Austria
University Hospitals Leuven
Leuven, Belgium
Shenyang Northern Hospital
Shenyang, China
Aarhus University Hospital
Aarhus, Denmark
Herzzentrum Bad Krozingen
Bad Krozingen, Germany
Segeberger Kliniken GmbH
Bad Segeberg, Germany
Charité Berlin, Campus Benjamin Franklin
Berlin, Germany
Start Date
September 1, 2008
Primary Completion Date
November 1, 2014
Completion Date
November 1, 2014
Last Updated
October 9, 2014
4,005
ACTUAL participants
Clopidogrel
DRUG
Placebo
DRUG
Lead Sponsor
Deutsches Herzzentrum Muenchen
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT01311323