Clinical Trials Directory

Trials / Completed

CompletedNCT00161070

ESPRIT: European/Australasian Stroke Prevention in Reversible Ischaemia Trial

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
4,500 (planned)
Sponsor
UMC Utrecht · Academic / Other
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Not accepted

Summary

The objective of ESPRIT was to compare the efficacy and safety of mild anticoagulation or a combination treatment of aspirin and dipyridamole with the efficacy and safety of treatment with aspirin alone after cerebral ischemia of arterial origin.

Detailed description

Low-dose aspirin (ASA) (at least 30 mg/day) prevents only 13% of subsequent vascular events after minor cerebral ischemia of arterial origin. Anticoagulation (AC) has been proven highly effective in preventing vascular events after myocardial infarction and after cerebral ischemia in patients with atrial fibrillation. A previous study on the effects of AC after cerebral ischemia of arterial origin (SPIRIT) showed that high intensity AC (INR 3.0 to 4.5) is not safe, but that mild AC (INR 2.0 to 3.0) was. The 2nd European Stroke Prevention Trial (ESPS-2) reported a 22% relative risk reduction of the combination of ASA and dipyridamole (DIP) above that of ASA only; its results, however, are subject to debate. Study design: ESPRIT was an open randomised controlled trial allocating patients who experienced a transient ischemic attack (TIA) or a non-disabling ischemic stroke to either: A. oral AC (INR 2.0 to 3.0); B. the combination of DIP (400 mg daily) plus ASA (30-325 mg/day); or C. ASA only (same dose). The mean follow-up was three years. Primary outcome was the composite of vascular death, stroke, myocardial infarction or major bleeding. Outcome assessment is blind.

Conditions

Interventions

TypeNameDescription
DRUGanticoagulation
DRUGaspirin and dipyridamole
DRUGaspirin alone

Timeline

Start date
1997-07-01
Completion
2006-12-01
First posted
2005-09-12
Last updated
2007-03-22

Locations

1 site across 1 country: Netherlands

Source: ClinicalTrials.gov record NCT00161070. Inclusion in this directory is not an endorsement.