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A double blind placebo controlled trial investigating the efficacy of Clopidogrel as prophylactic treatment for migrane. - Clopidogrel as prophylactic treatment for migrane

Phase 1
Conditions
Migraine
MedDRA version: 9.1Level: LLTClassification code 10027599Term: Migraine
Registration Number
EUCTR2008-001604-23-GB
Lead Sponsor
Guy's & St Thomas' NHS Foundation Trust
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Recruiting
Sex
All
Target Recruitment
286
Inclusion Criteria

Participants aged > 18
Definite migraine with or without aura as defined by International Headache criteria
Headache or aura occurring on 4 or more days and less than 15 days in a 28 day 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

High risk features suggesting cerebral malignancy,
More than 15 headache days each month
Contraindications to clopidogrel therapy (hypersensitivity, active bleeding, warfarin therapy, hepatic dysfunction)
Already prescribed clopidogrel (recent acute coronary syndrome, TIA with aspirin hypersensitivity)
Requirement for routine nonsteroidal anti-inflammatory agents (occaisional use is allowed)
Use of an investigational product within the previous 3 months
Clinically significant abnormal platelet or liver function at visit 1

Study & Design

Study Type
Interventional clinical trial of medicinal product
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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