N/A
N=18
Study of Laser Treatment of Melasma
Refractory Mixed Type Melasma
Bottom Line
View on ClinicalTrials.gov: NCT01335581 ↗Enrolled (actual)
18
Serious AEs
0.0%
Results posted
Dec 2020
Primary outcome: Primary: Melasma Area Severity Assessment (MASI) Score Change From Baseline to Follow Up — -5.6; 4.7 score on a scale
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- Q-Switched Nd:YAG Laser (RevLite) (Device); Retin-A and microdermabrasion (Drug)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- ConBio, a Cynosure Company
- Primary completion
- Mar 2012
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Melasma Area Severity Assessment (MASI) Score Change From Baseline to Follow Up |
-5.6; 4.7 | — |
Summary
The purpose of this study is to evaluate the RevLite laser in the treatment of refractory mixed type melasma.
Eligibility Criteria
Inclusion Criteria
- Fitzpatrick Skin Type III-VI
- mixed (epidermal and dermal) melasma diagnosed by Wood's Lamp exam
- age 18 or older
- melasma persisting for greater than 6 months that has failed to respond to conventional treatment with hydroquinone or other topical lightening agents
- written and verbal informed consent
- willing and able to comply with study instructions and return to the clinic for required visits
Exclusion Criteria
- Pregnancy, breastfeeding, taking birth control pills or plans to become pregnant during the study
- history of cutaneous photosensitization, porphyria, and hypersensitivity to porphyrins or photodermatosis
- any skin pathology or condition that could interfere with the evaluation or requires the use of interfering topical or systemic therapy
- uncorrected coagulation defect or is currently using anti-coagulation medication (including but not limited to heavy aspirin therapy)
- any condition which, in the investigator's opinion, would make it unsafe for the subject to participate in this research study
- currently enrolled in an investigational drug or device trial, or has received an investigational drug or has been treated with an investigational device within 30 days prior to entering this study
- inability to communicate or cooperate with the investigator due to language problems, poor mental development, or impaired cerebral function
- unreliability for the study (this includes subjects who engage in excessive alcohol intake or drug abuse, or subjects who are unable to return for scheduled follow-up visits)
- use of photosensitizing drugs within a timeframe where photosensitization from these drugs may still be present
- need to be exposed to artificial tanning devices or excessive sunlight during the trial
- Diabetes Type I or II
- sensitivity to hydroquinone or Retin-A
- evidence of a compromised immune system or hepatitis
- use of bleaching creams or retinoids within the last 30 days
Data sourced from ClinicalTrials.gov (NCT01335581). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.