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Compression and CO2 Laser for Leg Wounds
Sponsor: Northwestern University
Summary
The purpose of this study is to determine the efficacy and safety of compression bandaging with fractional ablative carbon dioxide laser (FACL) compared to compression and standard dressings alone for healing of post-operative wounds of the leg. This is a randomized, SMART design, clinical trial. Approximately 80 participants will be randomized to initially receive compression bandages or standard wound dressings after surgery on the lower leg. After 4 weeks, the group assigned to compression bandages will be further randomized to either continue with the compression bandages only or continue with the compression bandages and also receive (FACL). The study is designed as an 6-month study. This study was a pilot study designed to determine feasibility of these procedure. Subjects currently living in the Chicago metropolitan area and meet inclusion/exclusion criteria will be considered for enrollment.
Official title: Randomized, Investigator-blinded Study of Compression in Wound Healing With and Without Fractional Ablative CO2 Laser After Excisions on the Lower Extremity (CHIME+)
Key Details
Gender
All
Age Range
18 Years - Any
Study Type
INTERVENTIONAL
Enrollment
80
Start Date
2020-02-17
Completion Date
2025-06
Last Updated
2025-01-31
Healthy Volunteers
Yes
Conditions
Interventions
Compression bandages
Class I (20-30 mmHg) compression bandages or stocking
Standard wound dressings
Wound dressings alone consisting of gauze and skin tape to cover the wound
Fractional ablative carbon dioxide laser
Participant will have laser applied to their wound bed.
Locations (1)
Northwestern University Department of Dermatology
Chicago, Illinois, United States