drugset / Trial / NCT02239120

Dabigatran Etexilate for Secondary Stroke Prevention in Patients With Embolic Stroke of Undetermined Source (RE-SPECT ESUS)

NCT02239120 ↗

Phase 3 Completed 5390 enrolled Boehringer Ingelheim
RandomizedSingle-groupDouble-blindPrevention

Summary

This trial will enroll approximately 6,000 patients with recent embolic stroke of unknown source (ESUS). Patients will be randomized to dabigatran or acetylsalicyclic acid (ASA) (1:1 ratio) and have visits every three months. The study doctor may prescribe blinded concomitant ASA for pts with coronary artery disease but this is not mandatory. All Adverse Events (AEs), Serious Adverse Events (SAEs), outcome events will be recorded. The trial will conclude when the required number of stroke events are positively adjudicated which is estimated to take 3 years (including 2.5 years of enrollment).

Timeline

Start
2014-11-27
Primary completion
2018-08-14
Completion
2018-08-14

Outcome

Missed primary endpoint

registry analysis (superiority test); Dabigatran Etexilate 110 or 150 Milligram (mg) vs Acetylsalicylic Acid, Aspirin (ASA) 100 mg; p = 0.1028; Hazard Ratio (HR) 0.85 (95% CI 0.69 to 1.03); Regression, Cox NCT02239120 ↗

registry analysis (superiority test); Dabigatran Etexilate 110 or 150 Milligram (mg) vs Acetylsalicylic Acid, Aspirin (ASA) 100 mg; p = 0.1076; Hazard Ratio (HR) 1.36 (95% CI 0.94 to 1.97); Regression, Cox NCT02239120 ↗

paper In patients with a recent history of embolic stroke of undetermined source, dabigatran was not superior to aspirin in preventing recurrent stroke. PMID 31091372 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Comparator Aspirin Small molecule 100 mg Oral
Subject Dabigatran etexilate Unknown 110 mg Oral
Subject Dabigatran etexilate Unknown 150 mg Oral
Background ASA Unknown — —

Indications