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LeucoPatch in Malleoli Ulcer Study (LiDMUS)

Primary Purpose

Diabetic Malleoli Ulcers, Malleoli Ulcers

Status
Unknown status
Phase
Not Applicable
Locations
International
Study Type
Interventional
Intervention
LeucoPatch
Sponsored by
Nordsjaellands Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Diabetic Malleoli Ulcers focused on measuring Malleoli ulcers, Diabetes, Healing, Dressing, LeucoPatch

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept 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

Sites / Locations

  • Bispebjerg hospitalRecruiting
  • Viborg SygehusRecruiting
  • Nordsjaellands HospitalRecruiting
  • Herlev-Gentofte HospitalRecruiting
  • Kolding SygehusRecruiting
  • Skaane University HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

LeucoPatch

Usual care followed by LeucoPatch

Arm Description

Treatment with usual ulcer care and LeucoPatch once weekly up til 24 weeks or until healing.

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.

Outcomes

Primary Outcome Measures

Healing of malleoli ulcer (YES/NO)
Confirmed by a blinded observer

Secondary Outcome Measures

Time to healing of malleoli ulcer
Weeks from Inclusion to Wound healing
Ulcer area reduction based on Image J measured on acetate drawing
Health related quality of life questionnaire SF12
Short Form 12 questionnaire (quality of life)SF-12
Health related quality of life questionnaire EQ-5D
Euroquol-D5 questionnaire(mood and function) EQ-5D
Pain at ulcer location
VAS Score (Visual Analogue Scale)
Z scores of combined plasma concentration of growth factors, cytokines and inflammatory markers

Full Information

First Posted
October 27, 2016
Last Updated
July 8, 2019
Sponsor
Nordsjaellands Hospital
Collaborators
Reapplix, Skane University Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT02958072
Brief Title
LeucoPatch in Malleoli Ulcer Study
Acronym
LiDMUS
Official Title
LeucoPatch in Malleoli Ulcer Study
Study Type
Interventional

2. Study Status

Record Verification Date
June 2018
Overall Recruitment Status
Unknown status
Study Start Date
November 2016 (undefined)
Primary Completion Date
March 2020 (Anticipated)
Study Completion Date
November 2020 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Nordsjaellands Hospital
Collaborators
Reapplix, Skane University Hospital

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
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.
Detailed 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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diabetic Malleoli Ulcers, Malleoli Ulcers
Keywords
Malleoli ulcers, Diabetes, Healing, Dressing, LeucoPatch

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Masking Description
Open Label
Allocation
Randomized
Enrollment
36 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
LeucoPatch
Arm Type
Experimental
Arm Description
Treatment with usual ulcer care and LeucoPatch once weekly up til 24 weeks or until healing.
Arm Title
Usual care followed by LeucoPatch
Arm Type
Active Comparator
Arm 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.
Intervention Type
Other
Intervention Name(s)
LeucoPatch
Intervention Description
LeucoPatch is an fully autologous growth factor-containing dressing
Primary Outcome Measure Information:
Title
Healing of malleoli ulcer (YES/NO)
Description
Confirmed by a blinded observer
Time Frame
up to 24 weeks of treatment
Secondary Outcome Measure Information:
Title
Time to healing of malleoli ulcer
Description
Weeks from Inclusion to Wound healing
Time Frame
24 weeks
Title
Ulcer area reduction based on Image J measured on acetate drawing
Time Frame
24 weeks
Title
Health related quality of life questionnaire SF12
Description
Short Form 12 questionnaire (quality of life)SF-12
Time Frame
week 0, week 12, and week 24
Title
Health related quality of life questionnaire EQ-5D
Description
Euroquol-D5 questionnaire(mood and function) EQ-5D
Time Frame
week 0, week 12, and week 24
Title
Pain at ulcer location
Description
VAS Score (Visual Analogue Scale)
Time Frame
week 0, week 6, week 12 and week 24
Title
Z scores of combined plasma concentration of growth factors, cytokines and inflammatory markers
Time Frame
24 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Lise Tarnow, Professor
Phone
+4548293074
Email
lise.tarnow@regionh.dk
First Name & Middle Initial & Last Name or Official Title & Degree
Magnus Löndahl, MD, PhD
Phone
+46702742773
Email
magnus.londahl@med.lu.se
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Lise Tarnow, Professsor
Organizational Affiliation
Nordsjaellands Hospital
Official's Role
Study Director
Facility Information:
Facility Name
Bispebjerg hospital
City
Kobenhavn
State/Province
Region Hovedstaden
ZIP/Postal Code
2400
Country
Denmark
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Bo Jørgensen, MD
Facility Name
Viborg Sygehus
City
Viborg
State/Province
Region Midt
ZIP/Postal Code
8800
Country
Denmark
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Annette L Hoegh, MD, PhD
Facility Name
Nordsjaellands Hospital
City
Hillerod
State/Province
Regionh
ZIP/Postal Code
3400
Country
Denmark
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jan Sørensen, MD
Facility Name
Herlev-Gentofte Hospital
City
Herlev
Country
Denmark
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Hans Gotlieb, PhD
Facility Name
Kolding Sygehus
City
Kolding
Country
Denmark
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Kim Houlind
First Name & Middle Initial & Last Name & Degree
Kim Houlind
Facility Name
Skaane University Hospital
City
Lund
Country
Sweden
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Magnus Löndahl

12. IPD Sharing Statement

Plan to Share IPD
No

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LeucoPatch in Malleoli Ulcer Study

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