← Back to Search

Procedure

1210nm axillary laser treatments for Excessive Underarm Sweating

N/A
Waitlist Available
Led By John P. Trafeli, MD
Research Sponsored by United States Naval Medical Center, San Diego
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be between 18 and 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 7 months
Awards & highlights

Study Summary

Primary axillary hyperhidrosis is a common idiopathic disorder of the eccrine sweat glands that interferes with daily activities and causes significant social distress. This pilot study is designed to evaluate the efficacy and histologic effects of the 1210nm diode laser for the treatment of axillary hyperhidrosis. Initial results may inform the design of an anticipated larger prospective controlled trial. Study participants will receive one laser treatment to one randomly-assigned axilla using the 1210 nm diode laser, and two treatments to the opposite axilla. Changes in sweating will be measured both by quantitative gravimetric analysis of sweat production and by expert panel evaluation of photographs of the starch-iodine test performed on each axilla. Participants will also be asked to subjectively classify the severity of their axillary sweating. These measures will be performed at pretreatment and at one, three, and six months following treatment. Biopsies of both axillae will be done before and two weeks after treatment to assess histologic changes to the eccrine gland and surrounding structures. Treatment of axillary hyperhidrosis with the 1210nm diode laser is a novel approach based on the unique absorption characteristics of this wavelength. We hypothesize that selective heating of lipids at the appropriate tissue level will impact adjacent eccrine glands typically seated at the dermo-hypodermal junction, leading to subjective and/or objective decreases in eccrine secretions. This type of treatment may offer an effective, non-invasive and safe alternative to current treatment modalities.

Eligible Conditions
  • Excessive Underarm Sweating

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~7 months
This trial's timeline: 3 weeks for screening, Varies for treatment, and 7 months for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
gravimetric analysis
modified starch-iodine test
subjective global assessment questionnaire

Trial Design

2Treatment groups
Experimental Treatment
Group I: 1210nm laser treatments to the axillaExperimental Treatment1 Intervention
two laser treatments left axilla and one treatment right axilla
Group II: 1210nm axillary laser treatmentsExperimental Treatment1 Intervention
two laser treatments right axilla and one treatment left axilla

Find a Location

Who is running the clinical trial?

Candela Corp.UNKNOWN
United States Naval Medical Center, San DiegoLead Sponsor
102 Previous Clinical Trials
22,706 Total Patients Enrolled
John P. Trafeli, MDPrincipal InvestigatorUnited States Naval Medical Center, San Diego

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

Who else is applying?

What state do they live in?
Illinois
How old are they?
18 - 65
What site did they apply to?
NMCSD
What portion of applicants met pre-screening criteria?
Met criteria
~1 spots leftby Apr 2025