CI

At a glance

ClinicalIndex Comparison Record
Phase 3Completed· 2,725 enrolled
Drug / intervention
Dabigatran Etexilate 110mg +8 moredrug
Likely dose
Dabigatran Etexilate 110mgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT02164864
NCT02164864Phase 3Completed

A Prospective Randomised, Open Label, Blinded Endpoint (PROBE) Study to Evaluate DUAL Antithrombotic Therapy With Dabigatran Etexilate (110mg and 150mg b.i.d.) Plus Clopidogrel or Ticagrelor vs. Triple Therapy Strategy With Warfarin (INR 2.0 - 3.0) Plus Clopidogrel or Ticagrelor and Aspirin in Patients With Non Valvular Atrial Fibrillation (NVAF) That Have Undergone a Percutaneous Coronary Intervention (PCI) With Stenting

Boehringer Ingelheim·interventional·Posted Jun 17, 2014·Updated Jul 31, 2018

In Brief

A Phase 3 clinical trial evaluating Dabigatran Etexilate 110mg, Warfarin 3mg, and 5 other interventions for Atrial Fibrillation and Percutaneous Coronary Intervention. Completed, enrolled 2,725 participants across 421 sites in 41 countries.

Detailed Summary

The main objective of this study is to compare a Dual Antithrombotic Therapy (DAT) regimen of 110mg dabigatran etexilate b.i.d. plus clopidogrel or ticagrelor (110mg dabigatran etexilate (DE) DAT) and 150mg dabigatran etexilate b.i.d. plus clopidogrel or ticagrelor (150mg DE-DAT) with a Triple Antithrombotic Therapy (TAT) combination of warfarin plus clopidogrel or ticagrelor plus Aspirin (ASA) \<= 100mg once daily (warfarin-TAT) in patients with Atrial Fibrillation that undergo a PCI with stenting (elective or due to an Acute Coronary Syndrome). The study aims to show non-inferiority of each dose of DE-DAT when compared to Warfarin-TAT in terms of safety. Safety will be determined by comparing the rates of bleeding events, assessed using the modified International Society of Thrombosis and Haemostasis classification of Major Bleeding and Clinically Relevant Non Major Bleeding Events.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesArgentina, Australia, Austria, Belgium, Brazil, Bulgaria, Canada, Chile, Colombia, Croatia, Czechia, Denmark, Finland, France, Germany, Greece, Hong Kong, Hungary, India, Ireland, Israel, Italy, Japan, Mexico, Netherlands, New Zealand, Norway, Poland, Portugal, Russia, Singapore, Slovakia, Slovenia, South Korea, Spain, Sweden, Taiwan, Thailand, Turkey (Türkiye), United Kingdom, United States
Collaborators--

Timeline

Phase 3CompletedFinished
201520162017201820192020202120222023202420252026
First PostedJun 17, 2014
Enrollment StartJul 22, 2014
Primary CompletionJun 5, 2017
TodayJul 2, 2026
Enrollment to primary: 2.9 yearsPosted 12.0 years ago

Interventions

Dabigatran Etexilate 110mgdrug

Active treatment

Warfarin 3mgdrug

Active comparator

Aspirindrug

Active comparator

Dabigatran Etexilate 150mgdrug

Active treatment

Clopidogrel or Ticagrelordrug

Active comparator

Clopidogrel or Ticagrelordrug

Active comparator

Warfarin 5mgdrug

Active comparator

Clopidogrel or Ticagrelordrug

Active comparator

Warfarin 1mgdrug

Active comparator