Skip to content

Dual antiplatelet therapy in the acute phase following stroke and TIA; which is the best regimen?

Dual antiplatelet therapy in the acute phase following stroke and TIA; which is the best regimen?

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
EU CTR
Registry ID
EUCTR2007-002681-34-GB
Enrollment
60
Registered
2007-08-02
Start date
2007-09-28
Completion date
Unknown
Last updated
2019-11-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Symptomatic carotid artery stenosis MedDRA version: 9.1 Level: LLT Classification code 10007687 Term: Carotid artery stenosis

Interventions

Trade Name: Plavix Product Name: Clopidogrel Pharmaceutical Form: Tablet Trade Name: Persantin Product Name: Dipyridamole

Sponsors

St Georges Healthcare NHS Trust
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients with greater than or equal to 50% carotid artery stenosis AND symptoms of transient ischaemic attack or stroke within the last month. Are the trial subjects under 18? no Number of subjects for this age range: F.1.2 Adults (18-64 years) yes F.1.2.1 Number of subjects for this age range F.1.3 Elderly (>=65 years) yes F.1.3.1 Number of subjects for this age range

Exclusion criteria

Exclusion criteria: 1. antiplatelet/antithrombotic medication other than aspirin (although low does prophylactic subcutaneous heparin for DVT prophylaxis will be allowed) 2. patients with prosthetic heart valves who have gaseous embolic signals. 3. patients in who clopidogrel or dipyridamole are contraindicated. 4. If carotid endarterectomy is planned during the study.

Design outcomes

Primary

MeasureTime frame
Main Objective: Is clopidogrel plus aspirin, or dipyridamole slow release plus aspirin, a better combination in preventing embolisation in recently symptomatic large artery atherosclerotic disease?;Secondary Objective: ;Primary end point(s): Number of embolic signals during transcranial Doppler recording from ipsilateral middle cerebral artery performed at 48 hours after study entry

Countries

United Kingdom

Outcome results

None listed

Source: EU CTR (via WHO ICTRP) · Data processed: Feb 4, 2026