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Study of Laser Treatment of Melasma
NCT01335581 · View on ClinicalTrials.gov ↗
Study Summary
The purpose of this study is to evaluate the RevLite laser in the treatment of refractory mixed type melasma.
Conditions Studied
Interventions
- DEVICE Q-Switched Nd:YAG Laser (RevLite)
- DRUG Retin-A and microdermabrasion
Study Locations (1)
New York
- New York Laser and Skin Care — New York
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 18 participants |
| Start Date | 2011-04 |
| Est. Completion | 2012-03 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01335581
The ClinicalTrials.gov registry entry for NCT01335581 describes a study currently listed as completed. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 18 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is ConBio, a Cynosure Company, which has 2 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 1 condition, with Refractory Mixed Type Melasma appearing as the primary indexed condition, and to 2 interventions — of which Q-Switched Nd:YAG Laser (RevLite) is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT01335581 reports 1 study location spanning 1 distinct geographic area — top geographies include New York. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT01335581 about?
NCT01335581 is a clinical study titled "Study of Laser Treatment of Melasma". The purpose of this study is to evaluate the RevLite laser in the treatment of refractory mixed type melasma.
What is the current status of trial NCT01335581?
This trial is currently completed. It is a NA study. The enrollment target is 18 participants. The study started on 2011-04. Estimated completion is 2012-03.
What conditions does trial NCT01335581 study?
This clinical trial studies the following conditions: Refractory Mixed Type Melasma. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT01335581?
The interventions under investigation include: Q-Switched Nd:YAG Laser (RevLite) (DEVICE), Retin-A and microdermabrasion (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT01335581?
This trial is sponsored by ConBio, a Cynosure Company, which has 2 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT01335581 being conducted?
This trial has 1 study location across New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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