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Surgical Scar Treatment With the Pulsed Dye Laser in Combination With a CO2 Laser
NCT02898350 · View on ClinicalTrials.gov ↗
Study Summary
Prospective, randomized, split lesion treatment with 4 study Arms to evaluate safety and efficacy of combined treatment for minimizing of surgical scars, including post Moh's surgery.
Conditions Studied
Interventions
- DEVICE Pulsed dye laser treatment
- DEVICE CO2 laser treatment
- DEVICE Combined PDL and CO2 laser treatment
- DEVICE Split PDL and CO2 Laser treatment
Study Locations (2)
Colorado
- AboutSkin, Dermatology and Derm Surgery PC — Englewood
New York
- Laser & Skin Surgery Center of New York — New York
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 25 participants |
| Start Date | 2013-02 |
| Est. Completion | 2016-09 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT02898350
The ClinicalTrials.gov registry entry for NCT02898350 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 25 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Syneron Medical, 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 Scars appearing as the primary indexed condition, and to 4 interventions — of which Pulsed dye laser treatment 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: NCT02898350 reports 2 study locations spanning 2 distinct geographic areas — top geographies include Colorado, 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 NCT02898350 about?
NCT02898350 is a clinical study titled "Surgical Scar Treatment With the Pulsed Dye Laser in Combination With a CO2 Laser". Prospective, randomized, split lesion treatment with 4 study Arms to evaluate safety and efficacy of combined treatment for minimizing of surgical scars, including post Moh's surgery.
What is the current status of trial NCT02898350?
This trial is currently completed. It is a NA study. The enrollment target is 25 participants. The study started on 2013-02. Estimated completion is 2016-09.
What conditions does trial NCT02898350 study?
This clinical trial studies the following conditions: Scars. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT02898350?
The interventions under investigation include: Pulsed dye laser treatment (DEVICE), CO2 laser treatment (DEVICE), Combined PDL and CO2 laser treatment (DEVICE), Split PDL and CO2 Laser treatment (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT02898350?
This trial is sponsored by Syneron Medical, 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 NCT02898350 being conducted?
This trial has 2 study locations across Colorado, New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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