Evaluation of the Safety and Efficacy of the Pico Laser With a Specialized Lens Array for the Treatment of Wrinkles
Trial Snapshot
- Phase
- Not Applicable
- Status
- Completed
- Sponsor
- Cynosure, Inc.
- Enrollment
- 20
- Locations
- 1
- Primary Endpoint
- Photographic Evaluation of Wrinkle Severity at 4 Month Follow Up
Study Overview
Brief Summary
The purpose of this study is to evaluate the efficacy and safety of the treatment of wrinkles using the picosecond 755nm Alexandrite laser.
Study Design
- Study Type
- Interventional
- Allocation
- Na
- Intervention Model
- Single Group
- Primary Purpose
- Treatment
- Masking
- None
Eligibility Criteria
- Ages
- 18 Years to 65 Years (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •Is a healthy non-smoking (must have quit 1 year prior) male or female between 18 and 65 years old.
- •Is willing to consent to participate in the study.
- •Is willing to comply with all requirements of the study including biopsies, being photographed, following post treatment care and attending all treatment and follow up visits.
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.
- •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.
- •The subject has an allergy to lidocaine and epinephrine.
Arms & Interventions
755nm Alexandrite laser
755nm Alexandrite laser for the treatment of wrinkles
Intervention: 755nm Alexandrite laser (Device)
Outcomes
Primary Outcomes
Photographic Evaluation of Wrinkle Severity at 4 Month Follow Up
Time Frame: 4 months post last treatment
Blinded evaluators grade photographs using the Fitzpatrick wrinkle severity scale and provide an overall score for each timepoint. The Fitzpatrick wrinkle scale classifies wrinkles on a scale from 1 (mild) to 9 (severe).
Photographic Evaluation of Wrinkle Severity at Baseline
Time Frame: Baseline
Blinded evaluators grade photographs using the Fitzpatrick wrinkle severity scale and provide an overall score for each timepoint. The Fitzpatrick wrinkle scale classifies wrinkles on a scale from 1 (mild) to 9 (severe).
Photographic Evaluation of Wrinkle Severity at 1 Month Follow Up
Time Frame: 1 Month Follow Up Post Last Treatment
Blinded evaluators grade photographs using the Fitzpatrick wrinkle severity scale and provide an overall score for each timepoint. The Fitzpatrick wrinkle scale classifies wrinkles on a scale from 1 (mild) to 9 (severe).
Photographic Evaluation of Wrinkle Severity at 3 Month Follow Up
Time Frame: 3 Month Follow Up Post Last Treatment
Blinded evaluators grade photographs using the Fitzpatrick wrinkle severity scale and provide an overall score for each timepoint. The Fitzpatrick wrinkle scale classifies wrinkles on a scale from 1 (mild) to 9 (severe).
Photographic Evaluation of Wrinkle Severity at 6 Month Follow Up
Time Frame: 6 months post last treatment
Blinded evaluators grade photographs using the Fitzpatrick wrinkle severity scale and provide an overall score for each timepoint. The Fitzpatrick wrinkle scale classifies wrinkles on a scale from 1 (mild) to 9 (severe).
Secondary Outcomes
No secondary outcomes reported