Intraoperative CO₂ (Carbon Dioxide)
Part of paid clinical trials in Dallas, Texas.
- Sponsor
- Baylor Research Institute
- Study ID
- NCT07592468
- Status
- Not Yet Recruiting
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Conditions
- Wound Edges
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 89 Years
- Healthy Volunteers
- Not accepted
Interventions
- CO2 Fractionated Laser — DEVICEintraoperative fractionated CO₂ laser treatment of surgical wound edges
- Non CO2 Laser Treatment — PROCEDUREUntreated CO2 fractionated laser wound edges
Study Details
To evaluate whether intraoperative fractionated CO₂ laser treatment of surgical wound edges improves postoperative scar appearance compared with untreated wound edges following Mohs micrographic surgery (MMS).
Key Dates
- Start date
- May 31, 2026
- Status verified
- May 2026
- Primary completion
- Dec 31, 2027
- Completion
- Dec 31, 2027
Study Design
- Enrollment
- 50 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Active Comparator: CO2 Laser Treated Edge
- Active Comparator: Non-laser treated edge
Primary Outcome Measure
Improvement of postoperative scar appearance [ Time Frame: 3 months ]
Central Contacts
- Umer Nadir, MD214-820-2361
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Baylor University Medical Center | Dallas | Texas | 75246 | - |
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