Non-prescription Versus Prescription Topical Treatments Versus no Treatment in the Control of Sweating
This study has been completed.
Sponsor:
Northwestern University
Information provided by:
Northwestern University
ClinicalTrials.gov Identifier:
NCT00509886
First received: July 31, 2007
Last updated: May 25, 2011
Last verified: May 2011
- Full Text View
- Tabular View
- No Study Results Posted
- Disclaimer
- How to Read a Study Record
Purpose
Detailed Description:
The purpose of this study is to assess the effectiveness of the prescription treatment compared to the non-prescription treatment. It is hypothesized that the prescription treatment will have a significantly greater effect than the non-prescription treatment on decreasing excess sweating.
Condition | Intervention |
---|---|
Hyperhidrosis Excess Sweating |
Drug: Drysol Drug: Drioff |
Study Type: | Interventional |
Study Design: | Allocation: Randomized Endpoint Classification: Efficacy Study Intervention Model: Single Group Assignment Masking: Double Blind (Subject, Investigator) Primary Purpose: Prevention |
Official Title: | Non-prescription Versus Prescription Topical Treatments Versus no Treatment in the Control of Sweating |
Resource links provided by NLM:
Further study details as provided by Northwestern University:
Primary Outcome Measures:
- Gravimetric analysis [ Time Frame: 3 hours ] [ Designated as safety issue: No ]
Secondary Outcome Measures:
- Subject sweat assessment [ Time Frame: 3 hours ] [ Designated as safety issue: No ]
- HDSS [ Time Frame: 3 hours ] [ Designated as safety issue: No ]
Enrollment: | 24 |
Study Start Date: | June 2007 |
Study Completion Date: | August 2007 |
Primary Completion Date: | August 2007 (Final data collection date for primary outcome measure) |
Arms | Assigned Interventions |
---|---|
Experimental: 1
ARMs were randomized. One side of the body received treatment with one antiperspirant and the contralateral side with a different antiperspirant.
|
Drug: Drysol
20% aluminum chloride hexahydrate
|
Experimental: 2
ARMs were randomized. One side of the body received treatment with one antiperspirant and the contralateral side with a different antiperspirant.
|
Drug: Drioff
1% aluminum acetate
|
Detailed Description:
The objective of this study is to assess the effectiveness of the prescription treatment compared to the non-prescription treatment. It is hypothesized that the prescription treatment will have a significantly greater effect than the non-prescription treatment on decreasing excess sweating.
Eligibility
Ages Eligible for Study: | 21 Years to 30 Years |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | Yes |
Criteria
Inclusion Criteria:
- age 21-30 years
- males and females
- The subjects are in good health.
- The subjects have willingness and the ability to understand and provide informed consent for participation in the study.
Exclusion Criteria:
- Subjects with primary hyperhidrosis
- Subjects who are unable to withstand prolonged heat exposure or who have self-reported history of cardiovascular or respiratory disorders.
- Subjects who are unable to give informed consent.
- Subjects with mental illness.
- Subjects who are pregnant or nursing.
- Subjects with systemic or local skin disease and/or infection that may interfere with the conduct of the study.
Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00509886
Locations
United States, Illinois | |
Northwestern University Dermatology | |
Chicago, Illinois, United States, 60611 |
Sponsors and Collaborators
Northwestern University
Investigators
Principal Investigator: | Murad Alam, MD | Northwestern University dermatology |
Study Director: | Dennis West, PhD | Northwestern University dermatology |
More Information
No publications provided
Additional relevant MeSH terms:
ClinicalTrials.gov processed this record on October 17, 2012
No publications provided
Responsible Party: | Murad Alam, MD, Northwestern University Dermatology department |
ClinicalTrials.gov Identifier: | NCT00509886 History of Changes |
Other Study ID Numbers: | STU00000722 |
Study First Received: | July 31, 2007 |
Last Updated: | May 25, 2011 |
Health Authority: | United States: Institutional Review Board |
Additional relevant MeSH terms:
Hyperhidrosis Sweat Gland Diseases Skin Diseases Aluminum chloride Astringents |
Physiological Effects of Drugs Pharmacologic Actions Dermatologic Agents Therapeutic Uses |
ClinicalTrials.gov processed this record on October 17, 2012