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Non-prescription Versus Prescription Topical Treatments Versus no Treatment in the Control of Sweating

NCT00509886 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 24

Last updated 2014-11-10

No results posted yet for this study

Summary

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.

Conditions

  • Hyperhidrosis
  • Excess Sweating

Interventions

DRUG

Drysol

20% aluminum chloride hexahydrate

DRUG

Drioff

1% aluminum acetate

Sponsors & Collaborators

Principal Investigators

  • Murad Alam, MD · Northwestern University dermatology

  • Dennis West, PhD · Northwestern University dermatology

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
DOUBLE
Model
SINGLE_GROUP

Eligibility

Min Age
21 Years
Max Age
30 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2007-06-30
Primary Completion
2007-08-31
Completion
2007-08-31

Countries

  • United States

Study Locations

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Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00509886 on ClinicalTrials.gov