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Completed

NCT Number: NCT00161070

ESPRIT: European/Australasian Stroke Prevention in Reversible Ischaemia Trial

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.

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Key information

Age range

18 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

UMC Utrecht

Utrecht, Netherlands

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients presenting in the participating hospitals with a TIA or non-disabling stroke of atherosclerotic origin
  • Randomisation within 6 months after the TIA or minor stroke
  • Modified Rankin scale of 3 or less

Exclusion criteria

  • (Contra)indication to, or intolerance to, anticoagulants, dipyridamole, or aspirin
  • Disease expected to cause death within weeks or months
  • Source of embolism in the heart
  • Moderate or severe ischemic damage to the white matter of the brain (leukoaraiosis)
  • Anemia, polycythemia, thrombocytosis, or thrombocytopenia
  • Planned carotid endarterectomy
  • Intracranial bleeding or cerebral tumour
  • TIA or stroke caused by vasculitis, migraine, or dissection
  • Severe hypertension
  • Liver failure
  • Pregnancy
  • Chronic alcohol abuse

Treatment and study plan

anticoagulation

Drug

aspirin and dipyridamole

Drug

aspirin alone

Drug

Primary outcomes

  1. The combined event of death from all vascular causes, nonfatal stroke, nonfatal myocardial infarction or major bleeding complication, whichever happens first during follow-up

Secondary outcomes

  1. Death from all causes

  2. death from vascular causes

  3. death from vascular causes or nonfatal stroke

  4. fatal or nonfatal stroke

  5. death from vascular causes, nonfatal stroke, nonfatal myocardial infarction or vascular intervention

  6. major bleeding complications

  7. amputations of lower extremities

  8. retinal infarction or bleeding

Sponsors and collaborators

Lead sponsor

UMC Utrecht

Other

Registry information

Important dates

Study start
1997
Study completion
2006
First posted
Sep 12, 2005
Registry last updated
Mar 22, 2007

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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