Ticagrelor With Aspirin or Alone in High-Risk Patients After Coronary Intervention (TWILIGHT)
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|ClinicalTrials.gov Identifier: NCT02270242|
Recruitment Status : Completed
First Posted : October 21, 2014
Results First Posted : August 19, 2020
Last Update Posted : August 19, 2020
The purpose of this study is to compare the use of ticagrelor alone versus ticagrelor and aspirin together. Both ticagrelor and aspirin stop platelets from sticking together and forming a blood clot that could block blood flow to the heart. This study will look to determine the effectiveness and safety of ticagrelor alone, compared to ticagrelor plus aspirin in reducing clinically relevant bleeding and in reducing ischemic adverse events among high-risk patients who have had a percutaneous intervention with at least one drug-eluting stent. A patient is considered high-risk if they meet certain clinical and/or anatomic criteria.
Up to 9000 subjects will be enrolled at the time of their index PCI. Subjects meeting randomization eligibility criteria at 3 months post enrollment will be randomized to either ticagrelor plus aspirin or ticagrelor plus placebo for an additional 12 months. Follow-up clinic visits will be performed at 3 months, 9 months and 15 months post enrollment.
|Condition or disease||Intervention/treatment||Phase|
|Cardiovascular Disease Interventional Cardiology||Drug: Aspirin Drug: Placebo Drug: ticagrelor||Phase 4|
This is a multicenter, prospective, blinded dual-arm study. Up to 9000 high-risk patients who have undergone successful PCI with at least one locally approved drug eluting stent discharged on DAPT with aspirin and ticagrelor of at least 3 months intended duration from centers still to be determined in the U.S., Canada, Europe and Asia. The primary objective of this study is to determine the impact of antiplatelet monotherapy with ticagrelor alone versus DAPT with ticagrelor plus aspirin for 12 months in reducing clinically relevant bleeding (efficacy) among high-risk patients undergoing PCI who have completed a 3-month course of aspirin plus ticagrelor. The secondary objective of this study is to determine the impact of antiplatelet monotherapy with ticagrelor alone versus DAPT with ticagrelor plus aspirin for 12 months in reducing major ischemic adverse events (safety) among high-risk patients undergoing PCI who have completed a 3-month course of aspirin plus ticagrelor.
Exploratory objectives include assessing the comparative safety and efficacy of the different DAPT regimens for individual components of the primary efficacy and secondary safety objectives.
The primary analysis for TWILIGHT will be performed independently by the London School of Hygiene and Tropical Medicine
|Study Type :||Interventional (Clinical Trial)|
|Actual Enrollment :||9006 participants|
|Intervention Model:||Parallel Assignment|
|Masking:||Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)|
|Primary Purpose:||Supportive Care|
|Official Title:||Ticagrelor With Aspirin or Alone in High-Risk Patients After Coronary Intervention|
|Study Start Date :||July 2015|
|Actual Primary Completion Date :||July 10, 2019|
|Actual Study Completion Date :||July 10, 2019|
Active Comparator: Aspirin + Ticagrelor
enteric coated aspirin 81mg-100mg daily p.o. for 12 months and ticagrelor 90mg tablet bid for 12 months
Other Name: Ecotrin
Placebo Comparator: Placebo + Ticagrelor
placebo pill daily p.o. for 12 months - match for enteric coated aspirin 81mg-100mg and ticagrelor 90mg tablet bid for 12 months
- Number of Participants With BARC Type 2, 3, or 5 [ Time Frame: 12 months after randomization ]Number of participants with first occurrence of clinically relevant bleeding episode, defined as Bleeding Academic Research Consortium (BARC) Types 2, 3 or 5 bleeding. BARC bleeding types range from 0 (no bleeding) to 5 (fatal bleeding).
- Number of Participants With Ischemic Episode [ Time Frame: 12 months after randomization ]Number of participants with first occurrence of confirmed all-cause death, non-fatal myocardial infarction or stroke.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02270242
|United States, New York|
|Icahn School of Medicine at Mount Sinai|
|New York, New York, United States, 10029|
|Principal Investigator:||Roxana Mehran, MD||Icahn School of Medicine at Mount Sinai|
|Study Director:||Usman Baber, MD||Icahn School of Medicine at Mount Sinai|
|Study Chair:||Roxana Mehran, MD||Icahn School of Medicine at Mount Sinai|