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Clinical Trial 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).


Clinical Trial Description

n/a


Study Design

Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT01091129
Study type Interventional
Source Miramar Labs
Contact
Status Completed
Phase N/A
Start date February 2010
Completion date January 2012

See also
  Status Clinical Trial Phase
Completed NCT04546438 - Patient Satisfaction and Safety of Miradry Treatment for Axillary Hyperhidrosis N/A
Completed NCT03836287 - Safety and Efficacy Study of Sofpironium Bromide in Subjects With Axillary Hyperhidrosis (BBI-4000-CL-301) Phase 3
Enrolling by invitation NCT02105753 - Tx Axillary Hyperhidrosis 1210nm Diode Laser N/A
Withdrawn NCT05546710 - miraDry Post Market Tumescent Anesthesia Study N/A
Active, not recruiting NCT02295891 - Miradry Treatment for Focal Axillary Hyperhidrosis N/A
Completed NCT01118429 - Use of Oxybutynin to Treat Axillary Hyperhidrosis N/A
Completed NCT03948646 - Safety and Efficacy Study of Sofpironium Bromide in Subjects With Axillary Hyperhidrosis (BBI-4000-CL-302) Phase 3
Completed NCT01274611 - Botox and Suction-Curettage for Treatment of Excessive Underarm Sweating (Axillary Hyperhidrosis) N/A
Completed NCT03320096 - Evaluation of the Ulthera System for Treating Axillary Hyperhidrosis N/A
Completed NCT00735293 - VASER Treatment of Axillary Hyperhidrosis/Bromidrosis Phase 4