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Laser Therapy
LaseMD System for Melasma
N/A
Waitlist Available
Research Sponsored by LUTRONIC Corporation
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up from baseline to days 30, 90 and 180 following last treatment.
Awards & highlights
Study Summary
This study will evaluate the clinical outcomes associated with use of the LaseMD Laser System for the treatment of melasma.
Eligible Conditions
- Melasma
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ from baseline to days 30, 90 and 180 following last treatment.
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~from baseline to days 30, 90 and 180 following last treatment.
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Secondary outcome measures
Clinician assessment of overall aesthetic improvement.
Improvement in the Melasma Area and Severity Index (MASI) from Baseline
Improvement in the Melasma Quality of Life Scale (MELASQOL) from baseline
+3 moreTrial Design
1Treatment groups
Experimental Treatment
Group I: LaseMD SystemExperimental Treatment1 Intervention
Subjects will receive LaseMD System treatment(s) for treatment of melasma.
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Who is running the clinical trial?
LUTRONIC CorporationLead Sponsor
13 Previous Clinical Trials
551 Total Patients Enrolled
2 Trials studying Melasma
79 Patients Enrolled for Melasma
Kari Larson, MBAStudy DirectorSponsor GmbH
7 Previous Clinical Trials
416 Total Patients Enrolled
1 Trials studying Melasma
39 Patients Enrolled for Melasma
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