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Assessment of the Efficacy and Tolerance of Sub-cutaneous Re-injection of Autologous Adipose-derived REGEnerative Cells in the Local Treatment of Neuropathic Diabetic Foot ulcERs (REGENDER)

Primary Purpose

Diabetic Foot Ulcer

Status
Not yet recruiting
Phase
Phase 2
Locations
France
Study Type
Interventional
Intervention
adipose-derived regenerative cells (ADRCs)
Sponsored by
Assistance Publique Hopitaux De Marseille
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Diabetic Foot Ulcer

Eligibility Criteria

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

Inclusion Criteria:

  • Patient older than 18
  • Patient with type 1 or 2 diabetes mellitus with HbA1C level < 10%
  • Patient with diagnosis of neuropathic or neuro-ischemic DFU
  • Grade 1 or 2 ulcer on the Wagner scale
  • Ulcer with a surface area comprised between 1 cm2 and 15 cm2 at day 0 Patient present for a minimum of 4 weeks under the current investigator's care including adequate wound debridement and offloading
  • Semmes-Weinstein monofilament test indicating neuropathy
  • DFU located on the toe or on the lateral, dorsal surface of the forefoot or heel

Exclusion Criteria:

  • Pregnant or likely to become pregnant or breast feeding woman
  • Critical ischemia of the target limb, defined by pain at rest and an ankle systolic pressure < 50 mm Hg, or a toe systolic pressure < 30 mm Hg
  • Surgery or surgical revascularisation < 2months
  • Decrease or increase in the ulcer size by 30% or more within a 2-wk run-in period
  • DFU clinically infected as defined by the IDSA/IWGDF criteria, osteomyelitis confirmed by MRI, or other evidence of infection is present Dossier LIC-15-15-0005 REGENDER Déposé le 09/03/2015 15:22:11 par M. Patrice DARMON Appel LIC-15-2015 Page 3 sur 6
  • Patient who cannot bear an off-loading method
  • Patient with an active neoplasm

Sites / Locations

  • Assistance Publique Hopitaux de Marseille

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Diabetic foot ulcer

Arm Description

Outcomes

Primary Outcome Measures

Percentage of patients achieving 100% wound closure

Secondary Outcome Measures

time to reach complete wound closure
wound surface regression in relative value
wound surface regression in absolute value
percentage of patients achieving 50 % wound closure
ulcer recurrence rate
change in quality of life assessed by the SF-36 QoL survey from baseline

Full Information

First Posted
August 5, 2016
Last Updated
April 20, 2023
Sponsor
Assistance Publique Hopitaux De Marseille
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1. Study Identification

Unique Protocol Identification Number
NCT02866565
Brief Title
Assessment of the Efficacy and Tolerance of Sub-cutaneous Re-injection of Autologous Adipose-derived REGEnerative Cells in the Local Treatment of Neuropathic Diabetic Foot ulcERs
Acronym
REGENDER
Official Title
Assessment of the Efficacy and Tolerance of Sub-cutaneous Re-injection of Autologous
Study Type
Interventional

2. Study Status

Record Verification Date
April 2023
Overall Recruitment Status
Not yet recruiting
Study Start Date
June 2023 (Anticipated)
Primary Completion Date
September 2026 (Anticipated)
Study Completion Date
December 2026 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Assistance Publique Hopitaux De Marseille

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Diabetic foot ulcer (DFU) is a major complication and the leading cause of hospitalization among people with diabetes mellitus. It occurs in 15% of all patients with diabetes and precedes 84% of all lower leg amputations. Despite many therapeutic advances over the past decades, including dressings (hydrocolloids, alginate, skin substitutes) and growth factors, healing rates of DFU remain low. Mechanisms of faulty wound healing in diabetic patients are complex, related to both intrinsic and extrinsic factors. The main reasons for impaired healing appears to be: 1/exhaustion of local cell populations that promote wound healing; 2/excessive production of matrix metalloproteases (MMPs) coupled with reduced expression of the tissue inhibitors of MMPs; 3/impaired neovascularisation coupled with reduced numbers of endothelial progenitor cells and impairment of their functioning. These imbalances may result in excessive degradation of extracellular matrix components, as well as an inappropriate local inflammatory response . Adipose-derived stroma vascular fraction provides a rich and easily accessible source of autologous cells for regenerative medicine applications. Il contains multipotent stem cells and progenitors called adipose-derived regenerative cells (ADRCs) able to stimulate wound healing. There are attracted to the wound site where they supplement the wound bed with similar cell types, secrete numerous growth factors and cytokines, increase macrophage recruitment, enhance granulation tissue, and improve vascularisation . The reparative capabilities coupled with good safety of ADRCs have been illustrated in a study for treating severe and irreversible radiation-induced lesions, and in a study for treating sclerodactyly in patients with diffuse scleroderma. Numerous case reports showing healing of refractory wounds following treatment with autologous ADRCs have also been reported. Based on these previous reports, the present study aims to assess the efficacy and tolerance of injection of ADRCs for the local treatment of neuropathic or neuro-ischemic DFU.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diabetic Foot Ulcer

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
45 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Diabetic foot ulcer
Arm Type
Experimental
Intervention Type
Drug
Intervention Name(s)
adipose-derived regenerative cells (ADRCs)
Intervention Description
injection of the experimental treatment
Primary Outcome Measure Information:
Title
Percentage of patients achieving 100% wound closure
Time Frame
20 WEEKS
Secondary Outcome Measure Information:
Title
time to reach complete wound closure
Time Frame
20 WEEKS
Title
wound surface regression in relative value
Time Frame
20 weeks
Title
wound surface regression in absolute value
Time Frame
20 weeks
Title
percentage of patients achieving 50 % wound closure
Time Frame
20 weeks
Title
ulcer recurrence rate
Time Frame
20 weeks
Title
change in quality of life assessed by the SF-36 QoL survey from baseline
Time Frame
20weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patient older than 18 Patient with type 1 or 2 diabetes mellitus with HbA1C level < 10% Patient with diagnosis of neuropathic or neuro-ischemic DFU Grade 1 or 2 ulcer on the Wagner scale Ulcer with a surface area comprised between 1 cm2 and 15 cm2 at day 0 Patient present for a minimum of 4 weeks under the current investigator's care including adequate wound debridement and offloading Semmes-Weinstein monofilament test indicating neuropathy DFU located on the toe or on the lateral, dorsal surface of the forefoot or heel Exclusion Criteria: Pregnant or likely to become pregnant or breast feeding woman Critical ischemia of the target limb, defined by pain at rest and an ankle systolic pressure < 50 mm Hg, or a toe systolic pressure < 30 mm Hg Surgery or surgical revascularisation < 2months Decrease or increase in the ulcer size by 30% or more within a 2-wk run-in period DFU clinically infected as defined by the IDSA/IWGDF criteria, osteomyelitis confirmed by MRI, or other evidence of infection is present Dossier LIC-15-15-0005 REGENDER Déposé le 09/03/2015 15:22:11 par M. Patrice DARMON Appel LIC-15-2015 Page 3 sur 6 Patient who cannot bear an off-loading method Patient with an active neoplasm
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
PATRICE DARMON
Phone
+33491383653
Email
patrice.darmon@ap-hm.fr
First Name & Middle Initial & Last Name or Official Title & Degree
alexandra GIULIANI
Phone
+33491382747
Email
alexandra.giliani@ap-hm.fr
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
catherine GEINDRE
Organizational Affiliation
Assistance Publique Hopitaux De Marseille
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
PATRICE DARMON
Organizational Affiliation
Assistance Publique Hopitaux De Marseille
Official's Role
Principal Investigator
Facility Information:
Facility Name
Assistance Publique Hopitaux de Marseille
City
Marseille
Country
France
Facility Contact:
First Name & Middle Initial & Last Name & Degree
PATRICE DARMON
Email
patrice.darmon@ap-hm.fr
First Name & Middle Initial & Last Name & Degree
PATRICE DARMON

12. IPD Sharing Statement

Learn more about this trial

Assessment of the Efficacy and Tolerance of Sub-cutaneous Re-injection of Autologous Adipose-derived REGEnerative Cells in the Local Treatment of Neuropathic Diabetic Foot ulcERs

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