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ENROLLING BY INVITATION
NCT04198454
NA

Compression and CO2 Laser for Leg Wounds

Sponsor: Northwestern University

View on ClinicalTrials.gov

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

OTHER

Compression bandages

Class I (20-30 mmHg) compression bandages or stocking

OTHER

Standard wound dressings

Wound dressings alone consisting of gauze and skin tape to cover the wound

DEVICE

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