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Intranasal Civamide for Episodic Cluster Headache | Clinical Trials | Clareo Health

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COMPLETEDPhase 3NCT00069082

Intranasal Civamide for Episodic Cluster Headache

This is a 49-day study to evaluate the effectiveness of Intranasal Civamide (Zucapsaicin) in the treatment of an episodic cluster headache period compared to placebo (medically inactive substance whic...

Lead sponsor: Winston Laboratories•6 U.S. locations•View source on ClinicalTrials.gov

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Sponsors

Lead Sponsor

Winston Laboratories

Age

18 - No limit years

Sex

ALL

Healthy Volunteers

No

Inclusion Criteria

•At least 2 year history of episodic cluster headache (meeting IHS criteria)
•At least 2 previous episodes
•Expected duration of cluster period is at least 6 weeks but not longer than 24 weeks
•At least 1 but not more than 8 headaches on each of the 3 days immediately prior to treatment

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Data from ClinicalTrials.govLast updated on ClinicalTrials.gov: June 10, 2011Terms

Trial snapshot

StatusCOMPLETED

PhasePHASE3

Enrollment2

Start dateAug 2003

Last updatedJun 10, 2011

Condition

Episodic Cluster Headache

Locations shown

San Francisco Clinical Research Center

San Francisco, California

California Medical Clinic for Headache

Santa Monica, California

Colorado Neurology and Headache Clinic

Denver, Colorado

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Data Source & Attribution

This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

ClinicalTrials.gov last update: June 10, 2011Data synced to Clareo: May 25, 2026

Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.

Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.

View ClinicalTrials.gov Terms and Conditions