Clinical Trials Directory

Trials / Completed

CompletedNCT00184587

Prophylactic Treatment of Episodic Cluster Headache

Prophylactic Treatment of Episodic Cluster Headache With an Angiotensin II Receptor Blocker (Candesartan Cilexetil); a Randomized, Placebo Controlled Parallel Study

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
40 (actual)
Sponsor
Norwegian University of Science and Technology · Academic / Other
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Accepted

Summary

The purpose of this study is to determine whether candesartan cilexetil are effective prophylactic treatment of episodic Cluster headache

Detailed description

Cluster headache is an unilateral headache with periodic attacks, that usually lasts for 6 to 12 weeks. The pain is usually unbearable. The attacks are treated with injections of sumatriptan (migraine medication)and inhalation of oxygen. The most common prophylactics today has limited effect and a risk of side effects. Candesartan has in one study shown a clinically significant effect in migraine prophylaxis. The angiotensin II receptor blocker, candesartan is well tolerated with side-effects not significantly different from placebo and with few drug interactions. We therefore wish to investigate the prophylactic effect in treatment of cluster in headache patients. This will be a multicenter, double-blind, randomized, parallel study where the prophylactic effect of candesartan is compared to placebo in a period of 3 weeks. First week 16 mg and the following 2 weeks 32 mg.

Conditions

Interventions

TypeNameDescription
DRUGcandesartan cilexetil
DRUGplacebo

Timeline

Start date
2005-03-01
Primary completion
2009-06-01
Completion
2009-12-01
First posted
2005-09-16
Last updated
2013-04-23

Locations

1 site across 1 country: Norway

Source: ClinicalTrials.gov record NCT00184587. Inclusion in this directory is not an endorsement.