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NCT00004480 Clinical Trial

Study of Botulinum Toxin in Patients With Primary Hyperhidrosis

Hyperhidrosis Clinical Trial

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00004480
Other study ID # 199/14182
Secondary ID MTS-GCO-98-913NE
Status Completed
Phase N/A
First received October 18, 1999
Last updated June 23, 2005
Start date July 1999

Study information
Verified date July 2004
Source Office of Rare Diseases (ORD)
Contact n/a
Is FDA regulated No
Health authority Unspecified
Study type Interventional

Clinical Trial Summary

OBJECTIVES:

I. Determine the optimal dose of botulinum toxin necessary to decrease sweating in patients with primary hyperhidrosis.

Description:

PROTOCOL OUTLINE:

Patients receive injections of botulinum toxin in the clinical trial for 6 months. Patients undergo an iodine starch test and a sympathetic skin response test to assess the efficacy of the drug. Patients also complete questionnaires to evaluate the amount of sweating.

Recruitment information / eligibility
Status Completed
Enrollment 0
Est. completion date
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 16 Years and older
Eligibility - Diagnosis of hyperhidrosis

- Excessive sweating in the hands, feet, armpits, forehead, or body

Study Design

Primary Purpose: Treatment

Related Conditions & MeSH terms

Intervention

Drug:
• botulinum toxin type A

Locations
Country Name City State
United States Mount Sinai School of Medicine New York New York

Sponsors (1)
Lead Sponsor Collaborator
Icahn School of Medicine at Mount Sinai

Country where clinical trial is conducted

United States, 

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