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| Sponsor: | Winston Laboratories |
|---|---|
| Information provided by: | Winston Laboratories |
| ClinicalTrials.gov Identifier: | NCT00033839 |
Purpose
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 which does not contain any active ingredients).
| Condition | Intervention | Phase |
|---|---|---|
|
Episodic Cluster Headache |
Drug: Civamide (Zucapsaicin) |
Phase III |
| Study Type: | Interventional |
| Study Design: | Treatment, Randomized, Double-Blind, Placebo Control, Parallel Assignment, Safety/Efficacy Study |
| Official Title: | A Phase III, Double-Blind, Randomized, Placebo-Controlled, Parallel-Group, Multicenter Evaluation of Civamide (Zucapsaicin) Nasal Solution in the Treatment of Episodic Cluster Headache |
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Contacts and Locations
Show 26 Study Locations| Study Director: | Scott B. Phillips, M.D. | Winston Laboratories |
More Information
| Study ID Numbers: | WL-1001-02-02 |
| Study First Received: | April 11, 2002 |
| Last Updated: | June 23, 2005 |
| ClinicalTrials.gov Identifier: | NCT00033839 History of Changes |
| Health Authority: | United States: Food and Drug Administration |
|
Headache Cluster EC Episodic Cluster |
|
Cluster Headache Signs and Symptoms Trigeminal Autonomic Cephalalgias Nervous System Diseases Headache Neurologic Manifestations |
Central Nervous System Diseases Pain Headache Disorders, Primary Brain Diseases Headache Disorders |