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LeucoPatch in Malleoli Ulcer Study (LiDMUS)

N

Nordsjaellands Hospital

Status

Completed

Conditions

Diabetic Malleoli Ulcers
Malleoli Ulcers

Treatments

Other: LeucoPatch

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

An International Multicenter study evaluation, off the effect of the fully autologous growth factor-containing patch LeucoPatch, on healing of recalcitrant malleoli ulcers.

To compare the impact of LeucoPatch as part of usual care in multidisciplinary Foot clinic settings, versus usual care in the same clinics on malleoli ulcers healing.

Full description

Diabetic Foot Ulcers are a common and severe complication, that affects Patients Life Quality. Healing time is often long and the Diabetic foot ulcer is the dominating not traumatic reason for leg amputation.

Treatment of a diabetic foot ulcer requires debridement, offloading, regularly foot care, specially tailored shoes, antimicrobial treatment, and sometimes even surgical interventions. Despite all these interventions the diabetic foot ulcer may not heal.

Malleoli ulcers in patients without diabetes share several features of pathogenesis and lack of healing potentials with the Diabetic Ulcer. Like the features of pathogenesis and lack of healing potential and are therefore included in this study.

Research has shown that other methods such as Growth factors may be a way to enhance the chance of healing.

Growth Factors have been shown to have a positive effect in studies, but no products that are characterized as autologous have as yet obtained positive results in controlled studies.

LeucoPatch is produced solely from a patient´s own blood without addition, and is autologous. LeucoPatch appears as an elastic membrane and can be fitted to the individual ulcer.

LeucoPatch is shown to contain as many or more growth factors as existing products, and has a high concentration of fibrin, platelets and leukocytes.

A non-controlled study was made on ulcers less than 10cm 2 and 52% had competed epithelization after 20 weeks. An International randomized multicenter trial is ongoing to evaluate the efficacy and safety of LeucoPatch on healing of hard to heal diabetic foot ulcers below the malleoli.

This Study is designed to test the healing effect of the LeucoPatch on malleoli ulcers, the Patient will be randomized and the healing will be confirmed by a blinded observer.

Enrollment

20 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Foot ulcer at the malleoli area between 0,25 cm² and 5,0 cm²
  • Foot ulcer duration more than 6 weeks
  • No need for arterial revascularisation- as judged by the Investigator
  • informed consent

Exclusion criteria

  • Hemoglobin concentration under 6.5 mmol/l screening
  • Non-compliant with blood-letting
  • Clinically infected ulcer
  • Patient planned for or has had a revascularization procedure in the affected leg within the last 8 weeks
  • The ulcer have been treated with growth factors in the last 8 weeks
  • History of deep venous insufficiency, chronic venous leg ulcer or stasis dermatitis
  • Breast-feeding women or fertile women not agreeing to use an effective method of contraception
  • Participation in another clinical ulcer-healing study within the last 4 weeks
  • Patient has previously been randomized in this study
  • Judgement by the investigator that the patient is not able to participate in the study

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

20 participants in 2 patient groups

LeucoPatch
Experimental group
Description:
Treatment with usual ulcer care and LeucoPatch once weekly up til 24 weeks or until healing.
Treatment:
Other: LeucoPatch
Usual care followed by LeucoPatch
Active Comparator group
Description:
Usual care weekly for 12 weeks, if the ulcer persist after the12 weeks LeucoPatch treatment will be started for up to 12 weeks or until healing.
Treatment:
Other: LeucoPatch

Trial contacts and locations

6

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Central trial contact

Magnus Löndahl, MD, PhD; Lise Tarnow, Professor

Data sourced from clinicaltrials.gov

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