Trials / Completed
CompletedNCT00884663
Candesartan Versus Propranolol for Migraine Prevention
Candesartan vs Propranolol for Migraine Prevention: A Double Blind, Placebo Controlled, Double Dummy, Triple Cross-over Study
- Status
- Completed
- Phase
- Phase 2 / Phase 3
- Study type
- Interventional
- Enrollment
- 72 (actual)
- Sponsor
- Norwegian University of Science and Technology · Academic / Other
- Sex
- All
- Age
- 18 Years – 65 Years
- Healthy volunteers
- Not accepted
Summary
The main aim of the present study is to compare candesartan with propranolol for migraine prophylaxis.
Detailed description
Candesartan was shown to be effective for migraine prophylaxis in a randomized double blind cross-over study published in 2003. The drug is now widely used for this purpose in many countries, although no confirmatory study has been published. The aims of the present study are: 1) to see if the results in the first candesartan study can be replicated in a new patient population, including patients with chronic migraine, and, 2) to perform a head-to-head comparison of candesartan 16 mg/day with standard treatment with propranolol 160 mg slow release. We also intend to study whether responsiveness to these drugs may be related to heart rate variability and baroreceptor sensitivity.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Candesartan | Candesartan cilexitil tablets, 16 mg once daily |
| DRUG | propranolol | Propranolol hydrochloride capsules 160 mg once daily, slow release formulation |
| DRUG | placebo | placebo tablets and capsules |
Timeline
- Start date
- 2009-04-01
- Primary completion
- 2012-03-01
- Completion
- 2012-03-01
- First posted
- 2009-04-21
- Last updated
- 2013-12-24
Locations
1 site across 1 country: Norway
Source: ClinicalTrials.gov record NCT00884663. Inclusion in this directory is not an endorsement.