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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: ClinicalTrials.gov
Last refreshed on: 19 February 2015
Main ID:  NCT01402479
Date of registration: 24/07/2011
Prospective Registration: No
Primary sponsor: Seoul National University Hospital
Public title: An Open-labeled Trial of Ramipril in Patients With Migraine
Scientific title: An Open-labeled Trial of Ramipril in Patients With Migraine
Date of first enrolment: October 2004
Target sample size: 50
Recruitment status: Completed
URL:  http://clinicaltrials.gov/show/NCT01402479
Study type:  Interventional
Study design:  Allocation: Non-Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment  
Phase:  Phase 2
Countries of recruitment
Korea, Republic of
Contacts
Key inclusion & exclusion criteria

Inclusion Criteria:

- Patients with chronic migraine are included in this study. Migraineurs should be aged
20 to 70 years old with the ability to read and understand the self-report scales,
including the headache diary, used in this study.

Exclusion Criteria:

1. Medication overuse headache are excluded in this study.

2. Treatment with other ACEI or medication that may affect ARS

3. Treatment with migraine prophylactic medications or anti-hypertensive agents
including ß adrenergic receptor or calcium channel blockers

4. Past history of hepatic or renal dysfunction; an abnormal electrocardiography; a
psychiatric disorder; a history of substance abuse; pregnancy or lactation; use of
anti-psychotics, antidepressants, or anti-anxiety drugs.



Age minimum: 20 Years
Age maximum: 70 Years
Gender: Both
Health Condition(s) or Problem(s) studied
Migraine With Hypertension
Intervention(s)
Drug: Ramipril
Primary Outcome(s)
headache frequency [Time Frame: 12 week]
Secondary Outcome(s)
Secondary ID(s)
0408-131-005
Source(s) of Monetary Support
Please refer to primary and secondary sponsors
Secondary Sponsor(s)
Ethics review
Results
Results available:
Date Posted:
Date Completed:
URL:
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