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OpenTrials
Completed

NCT Number: NCT03796793

Developing Strategies for Effective Debridement in Patients for Venous Leg Ulcers

The goal of this project is to use genomic profiling, candidate genes and proteins to develop guided surgical debridement to improve healing in chronic non-healing venous leg ulcers (VLUs) and to test the efficacy of this approach.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University of Miami

Miami, Florida, 33136, United States

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • >18 years of age
  • Conformation of venous disease by non-invasive venous studies with either Doppler-confirmed venous reflux, or having ≥ 2 clinical characteristics of venous insufficiency (varicose veins, lipodermatosclersosis, venous dermatitis, atrophie blanche, edema)
  • have a venous ulcer between the knee and ankle, at or above the malleolus
  • wound size would be greater than or equal to 5cm2 in area without exposed tendon, muscle or bone
  • wound duration of at least 6 months
  • VLU containing yellow/white slough with or without fibrous/scar tissue and/or non-viable tissue
  • ability of subject to tolerate limb compression bandage

Exclusion criteria

  • history of diabetes mellitus and a HbA1c > 12% (obtained within past 6 months)
  • Ankle brachial index(ABI) less than 0.80
  • any active cancer other than a nonmelanoma skin cancer; any previous cancer must be in remission for at least 5 years
  • suspicion of malignancy within VLU
  • life expectancy <6 months
  • history of kidney disease and creatinine greater than 2.0 (obtained within past 6 months)
  • history of liver disease and liver function test (ALT, AST, ALK PHOS, and bilirubin) >2x upper limit of normal (obtained within past 6 months)
  • requirement for long-term systemic corticosteroids or immunosuppressive therapy, or history of corticosteroid or immunosuppressive use in the 4 weeks prior to study entry
  • history of immunodeficiency
  • ulcers due to none venous etiology and leg ulcers associated with mixed etiology
  • Untreated osteomyelitis
  • Hepatitis
  • acute deep venous thrombosis
  • allergy to lidocaine and/or epinephrine
  • Subject's inability to successfully tolerate compression therapy that is changed weekly
  • Skin ulcer previously treated within the last 4 weeks with biologic therapies (e.g. cell therapy or growth factors)
  • if currently incarcerated
  • known pregnancy

Treatment and study plan

Wound Edge Debridement

Procedure

Wound debridement is performed using a sharp, circular disposable curette to remove the slough, non-viable tissue and any fibrous tissue down to the vascular base.

Standard of Care Treatment

Other

Standard of Care treatment will include foam dressing and 4 layer compression therapy, changed weekly.

Primary outcomes

  1. Change in the Genetic Profile After Debridement in the Intervention Group.

    Time frame: Baseline and 4 weeks

    RNA sequencing will be used to determine the number of differentially expressed genes of the intervention group in samples collected pre-debridement to samples collected post-debridement.

Secondary outcomes

  1. Percent Rate of Healing Versus Non-healing Wounds Within Each Treatment Group

    Time frame: Baseline to 4 weeks

    Wound size is measured at every weekly visit. If the wound size decreased by 50% from baseline to week 4, the participant in considered having a "healing wound". If the wound size does not decreased by 50% from baseline to week 4, the participant is considered a "non-healing wound".

Sponsors and collaborators

Lead sponsor

University of Miami

Other

Collaborators

  • National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)

Registry information

Important dates

Study start
2019
Primary completion
2025
Study completion
2025
First posted
Jan 8, 2019
Registry last updated
May 14, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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