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 — DEVICE
    intraoperative fractionated CO₂ laser treatment of surgical wound edges
  • Non CO2 Laser Treatment — PROCEDURE
    Untreated 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

Locations (1)

FacilityCityStateZIPSite coordinators
Baylor University Medical CenterDallasTexas75246-

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