WithdrawnInterventionalNot ApplicableUpdated Feb 5, 2014
Evaluation of the 755nm Alexandrite Laser for Skin Toning and Epidermal Pigmented Lesions in Asian Skin Types | NCT01754246 | Trialant
CompletedInterventionalNot ApplicableUpdated Oct 27, 2020
Evaluation of the 755nm Alexandrite Laser for Skin Toning and Epidermal Pigmented Lesions in Asian Skin Types
ClinicalTrials.gov ID
NCT01754246
Lead Sponsor
Cynosure, Inc.INDUSTRY
Overall Status
Completed
Study Type
Interventional
Phase
Not Applicable
Enrollment
20Actual
Last Update Posted
Oct 27, 2020Actual
Start Date
Dec 2012
Primary Completion Date
Dec 2014Actual
Completion Date
Dec 2014Actual
Brief Summary
The purpose of this study is to assess treatment for facial skin toning and removal of epidermal pigmented lesions for Asian patients using the 755nm Alexandrite laser
Epidermal Pigmented Lesions
Skin Toning
755nm Alexandrite Laser
Ages Eligible for Study
Adult (18-64)Older Adult (65+)
Sexes Eligible for Study
All
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Is a healthy male or female between 18 and 85 years old
Has unwanted facial epidermal pigmented lesions or desires facial skin toning and wishes to undergo laser treatments.
Is willing to consent to participate in the study.
Is willing to comply with all requirements of the study including being photographed, following post treatment care and attending all treatment and follow up visits.
Has Fitzpatrick skin types III to IV.
Exclusion Criteria:
The subject is female and pregnant, has been pregnant within the last 3 months, is currently breast feeding or planning a pregnancy during the study period.
The subject is hypersensitive to light exposure OR takes photo sensitized medication.
The subject has active or localized systemic infections
The subject has a coagulation disorder, or is currently using anti-coagulation medication (including but not limited to heavy aspirin therapy {greater than 81 mg per day}).
The subject has any condition which, in the investigator's opinion, would make it unsafe for the subject to participate in this research study.
The subject is currently enrolled in an investigational drug or device trial, or has received an investigational drug or been treated with an investigational device within 3 months prior to entering this study.
The subject has used Accutane within 6 months prior to enrollment.
The subject has the need to be exposed to artificial tanning devices or excessive sunlight during the trial.
The subject has had prior treatment with parenteral gold therapy (gold sodium thiomalate).
The subject has a history of keloids or hypertrophic scarring.
The subject has evidence of compromised wound healing.
The subject has a history of squamous cell carcinoma or melanoma
The subject has a history of immunosuppression/immune deficiency disorders (including HIV infection or AIDS) or use of immunosuppressive medications.