Optimal Duration of Dual Antiplatelet Therapy After Drug-eluting Stent Implantation (OPTIDUAL)
Primary Purpose
Coronary Artery Disease, Stent Thrombosis, Myocardial Ischemia
Status
Completed
Phase
Phase 4
Locations
France
Study Type
Interventional
Intervention
Aspirin and Clopidogrel
Aspirin
Sponsored by
About this trial
This is an interventional treatment trial for Coronary Artery Disease focused on measuring Drug-eluting stent, Clopidogrel, Stent thrombosis, Myocardial infarction
Eligibility Criteria
Inclusion can be done either after stenting or 12 months later :
A: Patients admitted for DES implantation can be selected. After 12 months of bi therapy, they will be randomized
B: patients who have got a DES implantation 12 months before can be selected and randomised
Inclusion criteria:
- Patients on aspirin and clopidogrel therapy at 12 months after DES implantation
- Informed, written consent by the patient
Exclusion criteria:
- DES in left main coronary artery
- Oral anticoagulation therapy with coumadin derivatives
- Active bleeding; bleeding diathesis; history intracranial bleeding
- Known allergy or intolerance to the study medications: aspirin and clopidogrel
- Pregnancy (present, suspected or planned) or positive pregnancy test (In women with childbearing potential a negative pregnancy test is mandatory)
- Patient's inability to fully comply with the study protocol
Sites / Locations
- Hopital la Pitié Salpêtrière Institut de Cardiologie
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Active Comparator
Arm Label
1
2
Arm Description
Bi therapy : aspirin/ clopidogrel
Monotherapy: aspirin
Outcomes
Primary Outcome Measures
Composite criteria : death, non fatal myocardial infarction, non fatal stroke and severe bleeding
Secondary Outcome Measures
Death
Non fatal myocardial infarction
Non fatal stroke
Severe bleeding
Stent thrombosis (ARC définition)
Target lesion revascularization
Moderate bleeding (ISTH definition)
Full Information
NCT ID
NCT00822536
First Posted
January 13, 2009
Last Updated
October 16, 2014
Sponsor
Assistance Publique - Hôpitaux de Paris
Collaborators
Fédération Française de Cardiologie
1. Study Identification
Unique Protocol Identification Number
NCT00822536
Brief Title
Optimal Duration of Dual Antiplatelet Therapy After Drug-eluting Stent Implantation
Acronym
OPTIDUAL
Official Title
Optimal Duration of Dual Antiplatelet Therapy After Drug Eluting Stent (DES) Implantation
Study Type
Interventional
2. Study Status
Record Verification Date
October 2014
Overall Recruitment Status
Completed
Study Start Date
January 2009 (undefined)
Primary Completion Date
September 2014 (Actual)
Study Completion Date
September 2014 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Assistance Publique - Hôpitaux de Paris
Collaborators
Fédération Française de Cardiologie
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
To compare treatment with aspirin alone versus the combined antiplatelet treatment aspirin and clopidogrel after 12 months of combined antiplatelet treatment following drug-eluting stent (DES) implantation.
Detailed Description
Drug-eluting stents (DES) substantially reduce restenosis compared with bare metal stents and represent a significant advance in percutaneous coronary interventions (PCIs). Accordingly, DES have been rapidly adopted into practice and are currently used in the majority of PCI procedures. Despite their rapid acceptance, DES are not without limitations. In particular, patients who receive DES (like those who receive conventional bare metal stents) remain at risk of a 1% to 2% incidence of stent thrombosis, which is often associated with devastating consequences like death or myocardial infarction. Understanding and eliminating mediators of stent thrombosis are thus important goals for optimizing the clinical benefits of DES. Delayed endothelial coverage after DES implantation has been demonstrated and is thought to prolong the window of vulnerability to stent thrombosis. Consequently, current recommendations for DES are: dual antiplatelet therapy for at least 12 months in patients at low risk of bleeding, especially with " off-label " use. Because of rare but severe very late stent thrombosis, the dual antiplatelet therapy is more and more prescribed in clinical practice for several years.But it has been clearly demonstrated that the combination of aspirin and clopidogrel (the thienopyridine the most used) significantly increase the rate of severe and moderate bleedings when compared to aspirin alone. This is important if we consider the possibility or the necessity to prolong the combined antiplatelet therapy after stent implantation.ProposalTo compare treatment with aspirin alone versus the combined antiplatelet treatment with aspirin and clopidogrel after 12 months of combined antiplatelet treatment after DES implantation
NB : On the decision of the sponsor, the latest patient monitoring was advanced to September 30, 2014 instead of January 2015.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Coronary Artery Disease, Stent Thrombosis, Myocardial Ischemia
Keywords
Drug-eluting stent, Clopidogrel, Stent thrombosis, Myocardial infarction
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
1798 (Actual)
8. Arms, Groups, and Interventions
Arm Title
1
Arm Type
Active Comparator
Arm Description
Bi therapy : aspirin/ clopidogrel
Arm Title
2
Arm Type
Active Comparator
Arm Description
Monotherapy: aspirin
Intervention Type
Drug
Intervention Name(s)
Aspirin and Clopidogrel
Other Intervention Name(s)
Aspirin: acid acetylsalycilic, Clopidogrel: plavix
Intervention Description
Aspirin <= 325 mg/j Clopidogrel = 75 mg /j
Intervention Type
Drug
Intervention Name(s)
Aspirin
Other Intervention Name(s)
Aspirin: acid acetylsalycilic
Intervention Description
Aspirin : <= 325 mg/j
Primary Outcome Measure Information:
Title
Composite criteria : death, non fatal myocardial infarction, non fatal stroke and severe bleeding
Time Frame
At each visit (every 6 months) with Follow-up of 3 years
Secondary Outcome Measure Information:
Title
Death
Time Frame
At each visit (every 6 months) with Follow-up of 3 years
Title
Non fatal myocardial infarction
Time Frame
At each visit (every 6 months) with Follow-up of 3 years
Title
Non fatal stroke
Time Frame
At each visit (every 6 months) with Follow-up of 3 years
Title
Severe bleeding
Time Frame
At each visit (every 6 months) with Follow-up of 3 years
Title
Stent thrombosis (ARC définition)
Time Frame
At each visit (every 6 months) with Follow-up of 3 years
Title
Target lesion revascularization
Time Frame
At each visit (every 6 months) with Follow-up of 3 years
Title
Moderate bleeding (ISTH definition)
Time Frame
At each visit (every 6 months) with Follow-up of 3 years
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion can be done either after stenting or 12 months later :
A: Patients admitted for DES implantation can be selected. After 12 months of bi therapy, they will be randomized
B: patients who have got a DES implantation 12 months before can be selected and randomised
Inclusion criteria:
Patients on aspirin and clopidogrel therapy at 12 months after DES implantation
Informed, written consent by the patient
Exclusion criteria:
DES in left main coronary artery
Oral anticoagulation therapy with coumadin derivatives
Active bleeding; bleeding diathesis; history intracranial bleeding
Known allergy or intolerance to the study medications: aspirin and clopidogrel
Pregnancy (present, suspected or planned) or positive pregnancy test (In women with childbearing potential a negative pregnancy test is mandatory)
Patient's inability to fully comply with the study protocol
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Gérard HELFT, MD,PhD
Organizational Affiliation
Assistance Publique - Hôpitaux de Paris
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hopital la Pitié Salpêtrière Institut de Cardiologie
City
Paris
ZIP/Postal Code
75010
Country
France
12. IPD Sharing Statement
Citations:
PubMed Identifier
26364288
Citation
Helft G, Steg PG, Le Feuvre C, Georges JL, Carrie D, Dreyfus X, Furber A, Leclercq F, Eltchaninoff H, Falquier JF, Henry P, Cattan S, Sebagh L, Michel PL, Tuambilangana A, Hammoudi N, Boccara F, Cayla G, Douard H, Diallo A, Berman E, Komajda M, Metzger JP, Vicaut E; OPTImal DUAL Antiplatelet Therapy Trial Investigators. Stopping or continuing clopidogrel 12 months after drug-eluting stent placement: the OPTIDUAL randomized trial. Eur Heart J. 2016 Jan 21;37(4):365-74. doi: 10.1093/eurheartj/ehv481. Epub 2015 Sep 12.
Results Reference
derived
PubMed Identifier
23433461
Citation
Helft G, Le Feuvre C, Georges JL, Carrie D, Leclercq F, Eltchaninoff H, Furber A, Prunier F, Sebagh L, Cattan S, Cayla G, Vicaut E, Metzger JP. Efficacy and safety of 12 versus 48 months of dual antiplatelet therapy after implantation of a drug-eluting stent: the OPTImal DUAL antiplatelet therapy (OPTIDUAL) trial: study protocol for a randomized controlled trial. Trials. 2013 Feb 21;14:56. doi: 10.1186/1745-6215-14-56.
Results Reference
derived
Learn more about this trial
Optimal Duration of Dual Antiplatelet Therapy After Drug-eluting Stent Implantation
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