A Prospective Study of Axillary Hair Loss in Patients Treated With the miraDry System

Miramar Labs

Status: Completed

Conditions: Underarm Hair

Treatments: Device: miraDry Treatment

Study type: Interventional

Funder types: Industry

Identifiers

NCT01732497

CP-0009

Details and patient eligibility

About

The purpose of this study is to evaluate hair reduction in the underarms in patients treated with the miraDry System.

Full description

This study is designed to quantify the amount of hair reduction in patients treated with the miraDry System in the axilla. Hair counts will be assessed before and after treatments including at follow up visits.

Enrollment: 56 patients

Sex: All

Ages: 18+ years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• 18 years of age
• Visible underarm hair (prefer light colored hair; blonde, red, gray)

Exclusion criteria

• Secondary Axillary Hyperhidrosis
• Prior surgery and/or Botox Injections in axillae
• Pacemaker or requires supplemental oxygen
• Pregnant

Trial design

Primary purpose: Treatment

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

---

56 participants in 1 patient group

Single Group miraDry Treatment

Experimental group

Description:

This is a single group study where each enrolled subject will receive active miraDry treatment in each axilla.

Treatment:

Device: miraDry Treatment