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

Miramar Labs56 enrolled

Overview

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

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.

Study Type

INTERVENTIONAL

Allocation

Purpose

TREATMENT

Masking

NONE

Enrollment

Conditions

Underarm Hair

Interventions

miraDry TreatmentDEVICE

Application of electromagnetic energy to heat the lower dermis.

Eligibility

Sex: ALLMin age: 18 YearsHealthy volunteers:

Medical Language ↔ Plain English

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

Locations (3)

Zel Skin and Laser Specialists

Edina, Minnesota, United States

Laser & Skin Surgery Center of NY

New York, New York, United States

Lehigh Valley Dermatology

Bethlehem, Pennsylvania, United States

Outcomes

Primary Outcomes

Patients with successful hair reduction

Percentage of patients that show a \>=30% reduction in underarm hair at the 3 month visit compared to baseline.

Time frame: 3 months

Secondary Outcomes

Patients with successful hair reduction

Percentage of patients that achieve a \>=30% reduction in underarm hair at the 12 month visit compared to baseline

Time frame: 12 months

Data from ClinicalTrials.gov

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