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NCT02898350 · ClinicalTrials.gov registry record · NA

Surgical Scar Treatment With the Pulsed Dye Laser in Combination With a CO2 Laser

A NA study of Scars, sponsored by Syneron Medical.

Completed
Registry status
NA
Development phase
25
Enrollment target
2
Study locations

NCT02898350 is a NA study of Scars that has completed, run by Syneron Medical. The registered enrollment target is 25 participants, below the 231-participant average among 4 other Scars trials with a reported enrollment target (89% lower). The trial reports 2 study locations across 2 states.

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The verdict

NCT02898350, a NA study of Scars, has completed, sponsored by Syneron Medical.

COMPLETED
Registry status
NA
Development phase
25 participants
Enrollment target
2
Study locations

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

FieldValue
Enrollment Target 25 participants
Start Date 2013-02
Est. Completion 2016-09
Phase NA

Sponsor

Syneron Medical

18 total trials

What the Registry Record Tells You About NCT02898350

The ClinicalTrials.gov registry entry for NCT02898350 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 25 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 231-participant average among 4 other Scars trials with a reported enrollment target (89% lower). The listed sponsor is Syneron Medical, which has 18 total studies on file at ClinicalTrials.gov.

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.

NCT02898350 reports 2 study locations spanning 2 distinct geographic areas - top geographies include Colorado, New York.

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.

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).

Who is sponsoring clinical trial NCT02898350?

This trial is sponsored by Syneron Medical, which has 18 total clinical trials registered on ClinicalTrials.gov.

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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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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