755nm Alex Laser for Treatment of Pigmented and Vascular Lesions and Scars
Completed · Not applicable
Conditions studied: Benign Pigmented and Vascular Lesions and Scars
In brief
Evaluation of the safety and efficacy of the 755nm Alex laser for the treatment of benign pigmented and vascular lesions and scars
Key facts
- Study ID
- NCT01745627
- Run by
- Cynosure, Inc.
- People needed
- 43
- Starts
- 2011-10-01
- Expected to finish
- 2013-12-01
- Last updated by the study team
- 2020-12-23
Who can join
Age: 18 and older, up to 85. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Healthy male or female subjects between 18 and 85 years of age.
- Subjects with Fitzpatrick skin types I to VI.
- Subjects who have unwanted pigmented lesions, vascular lesions, striae and/or hypertrophic or atrophic scars
- Subject who are willing to consent to participate in the study.
- 2 Exclusion Criteria
- Subject who will not be photographed or who will not cooperate with the post treatment care and follow up schedule
- Hypersensitive to light exposure.
- Active localized or systemic infections.
- Taking medication for which sunlight is a contraindication.
- History of squamous cell carcinoma or melanoma.
- History of keloid scarring.
- Use of oral isotretinoin (Accutane®) within 12 months of initial treatment or during the course of the study. Note: Skin must regain its normal degree of moisture prior to treatment.
- Prior treatment with laser or other devices in treatment area within 3 months
- History of immunosuppression/immune deficiency disorders (including HIV infection or AIDS) or use of immunosuppressive medications.
- Subjects who are pregnant, have been pregnant within the last 3 months, are currently breast feeding or are planning a pregnancy within the study period.
- Subjects that the physician determines ineligible based on standard of care treatment.
Where it is running
- Laser & Skin Surgery Center of New York — New York, New York, United States
Full record on ClinicalTrials.gov
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