NCT06655129 Intense Pulsed Light (IPL) Medical Device as Treatment for Patient Suffering From Skin Disorder
| NCT ID | NCT06655129 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Eurofeedback |
| Condition | Excessive Hairiness |
| Study Type | INTERVENTIONAL |
| Enrollment | 85 participants |
| Start Date | 2024-01-20 |
| Primary Completion | 2024-12-30 |
Eligibility & Interventions
Eligibility Fast-Check
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What to Expect as a Participant
You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.
This trial targets 85 participants in total. It began in 2024-01-20 with a primary completion date of 2024-12-30.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief Summary
The first IPL device obtained United States Food and Drug Administration (FDA) clearance in 1995 for treatment of lower extremity telangiectasias. Since then, its favorable cost and versatility in contrast to many singlespectrum lasers, has led to its rapid proliferation and use in a number of different clinical settings. As described in the literature, ANTHÉLIA medical device is intended to treat skin disorders: * Excessive Hairiness (Hirsutism, Hypertrichosis...) * Vascular lesions (Rosacea….) * Pigmented lesions (Lentigo et melasma) * Acne vulgaris
Eligibility Criteria
Inclusion Criteria: * Adult men or women * Excessive Hairiness: * Patient with unwanted hair on the body (legs, arms, bikini line, or axilla) * Patient over 18 years. * Patients with Fitzpatrick skin types from I to V. * Women were required to be post-menopausal, surgically sterilized, or under a medically acceptable form of birth control (i.e., oral contraceptives, IUD, contraceptive implant, or barrier methods with spermicide or abstinence) during the study time period. Vascular lesions: * Patients over 18 years. * Patients with Fitzpatrick skin types from I to IV. * Patients with varicosities and Rosacea on the face or upper and lower limbs. Pigmented lesions: * Patients over 18 years. * Patients with solar lentigines on their cheeks, back, hands, arm and leg (\> 3 mm). * Patient with Fitzpatrick skin type from I to IV. Acne: * Patients over 18 years * Patients with Fitzpatrick skin types from I to IV. * Patients with facial acne vulgaris on face. * Willing to sun protect treated area for the duration of enrollment in the study and 4 weeks after treatment. Exclusion Criteria: * Patients with history of malignant lesions or pre-malignant lesions, scarring, or infection in the area to be treated History of keloidal or hypertrophic scarring * Patients with a known photosensitivity * Pregnancy women * Patient with diabetes mellitus suntan in the area to be treated * Use of photo-sensitizing products for 7 days before treatment (selftanning lotions, activators, self-tanning shower gel, etc.) * Exposure to the sun or UV rays at least 4 weeks before the treatment and 1 week afterwards * Zones with uncovered tattoos, suspect spots or skin diseases (including spots, inflammation, beauty spots, tumors or melanomas, psoriasis, herpes...) * Use of medication that induces anticoagulative medication or thromboembolic condition * Patients with pacemaker or internal defibrillator * Patients that used of NSAIDS two weeks prior to or 2 weeks following the treatment * Epileptic patients * Additional criteria for excessive hair: Patients that use waxing or other methods of photo epilation within 1 month prior to treatment. * Additional criteria for acne: Patients currently under oral antibiotic or oral therapy for acne.
Contact & Investigator
Frequently Asked Questions
Who can join the NCT06655129 clinical trial?
This trial is open to participants of all sexes, aged 18 Years or older, studying Excessive Hairiness. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT06655129 currently recruiting?
Yes, NCT06655129 is actively recruiting participants. Contact the research team at s.qualite@eurofeedback.com for enrollment information.
Where is the NCT06655129 trial being conducted?
This trial is being conducted at Auxerre, France, Brest, France, Nice, France, Périgueux, France and 1 additional location.
Who is sponsoring the NCT06655129 clinical trial?
NCT06655129 is sponsored by Eurofeedback. The trial plans to enroll 85 participants.