Pilot Study of Laser Hair Depilation for Pilonidal Disease

Status Completed

Clinical Trial Summary

Pilot study to assess tolerability and safety of laser hair depilation in adolescents and young adults with pilonidal disease.

Clinical Trial Description

This is a pilot study to measure safety and tolerance of laser hair depilation in adolescents and young adults with pilonidal disease as a potential treatment to intervene on future recurrence.

Up to a total of 10 patients will be enrolled.

Each patient will be involved in the study for one year. Patients will be brought into Surgery clinic for 1 laser treatment every 4-6 weeks to obtain a total of 5 treatments. Follow up will occur monthly from the time of initial treatment through 1 year after the last treatment as we evaluate for tolerance and efficacy.

Inclusion Criteria

- English and non-English speaking patients

- All Fitzpatrick skin types

- Age : 12-20 years

- Diagnosis of pilonidal disease

Exclusion Criteria

- History of photosensitivity

- Actively inflamed pilonidal sinus

Laser depilation treatment: Patients will be brought into Surgery clinic for 1 treatment every 4-6 weeks to obtain a total of 5 treatments. The treatment will consist of an 810 nm or Nd:YAG depending on Fitzpatrick skin type and tolerability. A cooling platform and application of topical lidocaine cream will be used to minimize any discomfort associated with the heat of the laser treatments.

Initial follow up for the laser depilation group will be performed to assess for tolerance of the laser treatment. Patients will report their pain every 6 hours for the first 48 hours after their laser hair depilation treatment. Once tolerance is established, patients will return to surgical clinic every month for their laser or placebo visit. After the 5th clinic visit, they will receive a telephone call monthly to assess for any evidence of resolution or recurrence of disease up to 1 year after the completion of the treatments. ;

Study Design

Related Conditions & MeSH terms

Pilonidal Disease

Clinical Trial Details

NCT number	NCT02778152
Study type	Interventional
Source	Nationwide Children's Hospital
Contact
Status	Completed
Phase	N/A
Start date	February 19, 2016
Completion date	February 2, 2018

View Details

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