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Clinical Evaluation of the miraDry System in Subjects With Hyperhidrosis

NCT01091129 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 31

Last updated 2014-12-09

No results posted yet for this study

Summary

The purpose of this study is to determine whether treatment by the miraDry System can safely reduce the severity of axillary hyperhidrosis (excessive underarm sweating).

Conditions

  • Axillary Hyperhidrosis

Interventions

DEVICE

miraDry System (treatment with energy)

Treatment with microwave energy delivery device as specified by manufacturer's instructions

Sponsors & Collaborators

  • Miramar Labs

    lead INDUSTRY

Principal Investigators

  • Chih-ho Hong, MD · Guildford Dermatology Specialists

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2010-02-28
Primary Completion
2011-01-31
Completion
2012-01-31

Countries

  • Canada

Study Locations

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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 NCT01091129 on ClinicalTrials.gov