Clinical Evaluation of Splendor X for Hair Removal

Status unconfirmed · Not applicable

Conditions studied: Hair Remval

In brief

At least 40 healthy male or female subjects that wish to remove their hair will be enrolled to this study. Each subject will receive five treatments at 6-8 weeks intervals. Subjects will return for follow-up visits at 3, 6, 9, and 12 months after the last treatment.

Key facts

Study ID

NCT04152707

Run by

Lumenis Be Ltd.

People needed

44

Starts

2020-01-08

Expected to finish

2023-04-01

Last updated by the study team

2021-07-02

Who can join

Age: 18 and older, up to 50. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Able to read, understand and provide written Informed Consent;
• All skin types: I-VI
• Male or female
• Age - 18-50 years of age
• Having one suitable treatment areas (legs, back, Chest or abdomen) with dark brown or black hair appropriate for hair removal;
• Interested in laser hair removal treatment for permanent hair reduction in the suitable area
• Able and willing to comply with the treatment/follow-up schedule and requirements;
• Women of child-bearing age are required to be using a reliable method of birth control at least 3 months prior to enrollment and throughout the course of the study.

You may not qualify if…

• Pregnant, expectation of pregnancy, postpartum or nursing (<6 months);
• Participation in another clinical study
• Active infections in the treated area;
• Dysplastic nevi in the treatment area;
• Tattoos in the treatment area;
• Current cancer, history of skin cancer or pre-cancerous lesions at the treatment areas;
• History of keloid scars anywhere on the body or scar formation in the treatment area ; or at risk of Keloid scars
• Active cold sores, open lacerations or abrasions in the treated area;
• Herpes simplex in the treatment area
• Prior skin treatment with laser or other devices on the same treated areas prior to study enrollment or during the course of the study
• Significant concurrent skin conditions or any inflammatory skin conditions;
• Chronic or cutaneous viral, fungal, or bacterial diseases;
• Intense tan, Deep suntan, recent suntan within 2 weeks, sunburn or artificially tanned skin;
• Use of medications, herbal supplements, perfumes or cosmetics that may affect sensitivity to light or change skin metabolism
• Skin lesions
• Bleeding coagulopathies or use of anticoagulants
• Hormonal disorders that may affect hair growth;
• Immunosuppressive diseases, including AIDS and HIV infection, or use of immunosuppressive medications; or other auto-immune dsorders.
• Livedo reticularis;
• Uncontrolled systemic diseases such as diabetes;
• Use of Accutane™ (Isotretinoin) within the past 6 month;
• Erythema ab igne, when identified treatments should be discontinued;
• Photosensitivity disorder that can be exacerbated by laser or intense light (such as Epilepsy).
• Poor wound healing;
• Unable or unlikely to refrain from artificial tanning, including the use of tanning booths, prior (at least 6 week) and during the course of the evaluation;

Where it is running

• SkinCare Physicians — Boston, Massachusetts, United States
• Union Square Laser Dermatology — New York, New York, United States

Full record on ClinicalTrials.gov

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