Clinical Evaluation of Hair Removal and Permanent Hair Reduction for Skin Types VI Using Intense … (NCT02452398) | Clinical Trial Compass
TerminatedNot Applicable
Clinical Evaluation of Hair Removal and Permanent Hair Reduction for Skin Types VI Using Intense Pulsed Light
Stopped: Study withdrawn as technology already proven with data no longer needed.
United States79 participantsStarted 2015-01
Plain-language summary
This is a Multi-center, blinded, baseline-controlled, prospective study to evaluate permanent hair reduction and removal for skin types V and VI using IPL.
Who can participate
Age range21 Years
SexALL
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion criteria
✓. Able to read, understand and provide written Informed Consent;
✓. Subject has black or dark brown terminal hairs in the areas to be treated.
✓. Terminal hair density requirement of greater than 15 hairs within the hair count site (3x3 cm area) as determined by manual hair count performed by the study investigator.
✓. Healthy adult, male or female, 21 years of age or older with skin type V-VI;
✓. Having a suitable treatment area for hair removal;
✓. Able and willing to comply with the treatment/follow-up schedule and requirements;
✓. Women of child-bearing potential (women who have not had a hysterectomy, bilateral oophorectomy or are not postmenopausal) are required to be using a reliable method of birth control at least three months prior to enrollment and throughout the course of the study.
Exclusion criteria
✕. Subject has light ,gray terminal or fine hairs in all/some parts of the treated area;
✕. Pregnant, expectation of pregnancy, postpartum or nursing (\<6 months);
✕. Hormonal disorders that may affect hair growth;
✕. Immunosuppressive diseases, including AIDS and HIV infection, or use of immunosuppressive medications;