Sunstone IPL (Intense Pulsed Light) for Hair Reduction

Status Completed

Clinical Trial Summary

This is a prospective, multi-center, single-arm, single blinded study to evaluate the safety and efficacy of the Sunstone IPL (Intense Pulsed Light) device to remove hair.

Clinical Trial Description

Prospective, multi-center, single-arm, single blinded (Philips hair counter) study in healthy women of skin types I up to and including V. Safety and efficacy of hair removal with the Investigational Philips IPL-device will be investigated. In-clinic, each study subject will undergo twelve IPL-treatments at four areas bilaterally (face, axilla, bikini line, and legs) with an investigational IPL device applied by a device operator. Hair re-growth in four body areas, face, axillae, bikini line and leg will be evaluated separately. After the 4 bi-weekly treatments, one follow-up visit will be organized. After the completion of full treatment cycle (12 treatments), subjects will be followed for 1 and 3 months (short-term follow-up) and for 6, 9 and 12 months (long-term follow up). ;

Study Design

Related Conditions & MeSH terms

Hair Removal

Clinical Trial Details

NCT number	NCT03921814
Study type	Interventional
Source	Philips Healthcare
Contact
Status	Completed
Phase	N/A
Start date	April 11, 2019
Completion date	May 20, 2022

View Details

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