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NCT02985151 · ClinicalTrials.gov registry record · NA
Interventional Study to Evaluate the Appearance of Surgical Scars After Laser Therapy
A NA study, sponsored by St. Louis University.
- Completed
- Registry status
- NA
- Development phase
- 51
- Enrollment target
NCT02985151 is a NA study that has completed, run by St. Louis University. The registered enrollment target is 51 participants.
The verdict
NCT02985151, a NA study, has completed, sponsored by St. Louis University.
- COMPLETED
- Registry status
- NA
- Development phase
- 51 participants
- Enrollment target
Study Summary
This study evaluates the effect of a fractionated carbon dioxide laser on surgical scars of the face and neck over 12 months. Anyone with a surgical scar on the face and neck who has not had laser therapy may be eligible to participate. The visits occur every three months for up to 12 months. Subjects will be randomly assigned to receive a higher energy treatment or a lower energy treatment during the study. Subjects and raters will be blinded to which therapy level the patient receives. At each visit, the scars will be photographed and the subject will complete a questionnaire to rate the scar prior to treatment. Three physicians will evaluate the scar at each visit. One rater will evaluate the scars in person during the visit, while the other two raters will evaluate the scars using photographs after each visit. During the first three study visits, subjects will receive their assigned treatment, obtain post-treatment instructions, and a diary to record redness, swelling, pain, itching, or other skin changes after treatment. At the third study visit, subjects will have the option to receive additional treatments or terminate their participation in the study. The fourth visit for those who continue will be a treatment visit for one group and the fifth visit will be for data collection, with no treatment offered.
Interventions
- DEVICE Syneron-Candela CO2RE Laser
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 51 participants |
| Start Date | 2016-11-01 |
| Est. Completion | 2020-12-01 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT02985151
The ClinicalTrials.gov registry entry for NCT02985151 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 51 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is St. Louis University, which has 107 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 1 intervention - of which Syneron-Candela CO2RE Laser is the first listed.
NCT02985151 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT02985151 about?
NCT02985151 is a clinical study titled "Interventional Study to Evaluate the Appearance of Surgical Scars After Laser Therapy". This study evaluates the effect of a fractionated carbon dioxide laser on surgical scars of the face and neck over 12 months. Anyone with a surgical scar on the face and neck who has not had laser therapy may be eligible to participate. The visits occur every three months for up to 12 months. Subjec...
What is the current status of trial NCT02985151?
This trial is currently completed. It is a NA study. The enrollment target is 51 participants. The study started on 2016-11-01. Estimated completion is 2020-12-01.
What interventions are being tested in trial NCT02985151?
The interventions under investigation include: Syneron-Candela CO2RE Laser (DEVICE).
Who is sponsoring clinical trial NCT02985151?
This trial is sponsored by St. Louis University, which has 107 total clinical trials registered on ClinicalTrials.gov.
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