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Treatment of Hypertensive Leg Ulcer by Adipose Tissue Grafting (Angiolipo)

Primary Purpose

Skin Ulcer

Status
Unknown status
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
adipose tissue grafting
Sponsored by
University Hospital, Caen
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Skin Ulcer focused on measuring necrotitis angiodermatitis, autologous fat transplantation, mesenchymal stem cells

Eligibility Criteria

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

Inclusion Criteria:

  • Patients over 18 years with a necrotic ulcer or angiodermatitis Martorell.
  • Recipient of the system of social security.
  • Ulceration sudden onset peripheral Livedoid border, on superficial leg without bone or tendon exposure.
  • IPS Index (systolic pressure)> 0.8 with pedal pulses.
  • Wound area less than 300 cm2 surface measurement with Canvas ® software from a photograph of the wound next to which there is a calibration strip.
  • Patients with hypertension.
  • Patient was informed of the study and having signed an informed consent.

Exclusion Criteria:

  • Severe distal arteritis (arteritis of large arteries).
  • Histological vasculitis.
  • Collagen (THE BY, scleroderma).
  • Blood Pathology: Cryoglobulinemia, Polycythemia.
  • Hepatitis A, B and C, HIV and syphilis infection
  • Thrombophilia (search for markers during the initial assessment in patients with a history of phlebitis or miscarriage).
  • Hyperthyroidism.
  • Patient treated with Hydrea (favoring the occurrence of ulcers).
  • Patient participating in another study to treat the wound concerned.
  • Topics minors, pregnant women, persons deprived of liberty, adults under legal protection unable to consent.

Sites / Locations

  • University Hospital, CaenRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

adipose tissue grafting

Arm Description

Outcomes

Primary Outcome Measures

Treatment of hypertensive leg ulcer by adipose tissue grafting
The objective of this study is to evaluate pain

Secondary Outcome Measures

treatment of angiodermatitis necrotitis by lipofilling
Other objectives are to evaluate the tolerance, in terms of pain and side effects, and secondly, the effectiveness of this therapeutic approach, in terms of healing of the ulcer assuming a decrease in the size of the estimated at least 40% at 3 months wound. The objective also covers the measurement of changes in the appearance of the wound, with an expected decrease of relative areas of fibrin and necrosis. The percentage of wound healing and wound area was measured at each visit, a curve will be performed for each patient to assess the speed of healing and the appearance of the wound will be notified.

Full Information

First Posted
April 18, 2013
Last Updated
April 8, 2014
Sponsor
University Hospital, Caen
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1. Study Identification

Unique Protocol Identification Number
NCT01932021
Brief Title
Treatment of Hypertensive Leg Ulcer by Adipose Tissue Grafting
Acronym
Angiolipo
Official Title
Treatment of Hypertensive Leg Ulcer by Adipose Tissue Grafting
Study Type
Interventional

2. Study Status

Record Verification Date
April 2014
Overall Recruitment Status
Unknown status
Study Start Date
April 2013 (undefined)
Primary Completion Date
April 2014 (Anticipated)
Study Completion Date
December 2014 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Hospital, Caen

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The hypertensive leg ulcer is a very painful leg related to acute skin microangiopathy. It occurs in patients older than 60 years followed for hypertension. Clinical diagnosis requires eliminating other causes arterial ulcers, cryoglobulinemia, thrombophilia, cholesterol crystal emboli, vasculitis associated with hepatitis C, myeloproliferative disorders and ulcers associated with the Hydrea ® outlet. There is no treatment of the ulcer because conventional treatments are ineffective. The pain has subsided by analgesics III. Other treatments are not effective outside skin grafts to be repeated because they necrotic regularly. In a prospective uncontrolled study, 11 patients healed through autohemotherapy. Ineffective treatment of this painful condition and efficiency of these cells to the damaged tissue, due to the secretion of many bioactive molecules, led us to propose subcutaneous injections of autologous fat to change the wound bed, promote healing and eliminate pain. This treatment should help to avoid long-term hospitalization (about 15 days) that can lead to physical and psychological degradation of these elderly patients. The investigators propose an open clinical study of 10 patients with a single-center recruitment (CHU Caen). The study took place over a period of 18 months with a 12-month recruitment and follow-up of 6 months for each patient. The purpose of this study was to evaluate the one hand, tolerance, in terms of pain and side effects, and, on the other hand, the effectiveness of this therapeutic approach, in terms of healing of the ulcer assuming a decrease in the size of the estimated at least 40% at 3 months wound. The measure of effectiveness will also focus on the changing appearance of the wound, including the relative areas of fibrin, necrosis and budding. These efficiency measures (area ratio) will be done through a computer program (CANVAS ®) on photographs taken at each assessment time. Eventually, if this study was to demonstrate the effectiveness of this treatment lipofilling, it would be possible to perform a multicenter study on a large number of patients to demonstrate the effectiveness, in terms of wound healing that the pain it causes and offer a shorter hospital stay, and in parallel, this approach should improve the pathophysiology of ulceration (translational research).
Detailed Description
The objective of this study was to evaluate the one hand, tolerance, in terms of pain and side effects, and secondly, the effectiveness of this therapeutic approach, in terms of healing of the ulcer assuming a decrease in the size of the estimated at least 40% at 3 months wound. The objective also covers the measurement of changes in the appearance of the wound, with an expected decrease of relative areas of fibrin and necrosis. The percentage of wound healing and wound area was measured at each visit, a curve will be performed for each patient to assess the speed of healing and the appearance of the wound will be notified.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Skin Ulcer
Keywords
necrotitis angiodermatitis, autologous fat transplantation, mesenchymal stem cells

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
10 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
adipose tissue grafting
Arm Type
Experimental
Intervention Type
Procedure
Intervention Name(s)
adipose tissue grafting
Primary Outcome Measure Information:
Title
Treatment of hypertensive leg ulcer by adipose tissue grafting
Description
The objective of this study is to evaluate pain
Time Frame
one year
Secondary Outcome Measure Information:
Title
treatment of angiodermatitis necrotitis by lipofilling
Description
Other objectives are to evaluate the tolerance, in terms of pain and side effects, and secondly, the effectiveness of this therapeutic approach, in terms of healing of the ulcer assuming a decrease in the size of the estimated at least 40% at 3 months wound. The objective also covers the measurement of changes in the appearance of the wound, with an expected decrease of relative areas of fibrin and necrosis. The percentage of wound healing and wound area was measured at each visit, a curve will be performed for each patient to assess the speed of healing and the appearance of the wound will be notified.
Time Frame
one year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients over 18 years with a necrotic ulcer or angiodermatitis Martorell. Recipient of the system of social security. Ulceration sudden onset peripheral Livedoid border, on superficial leg without bone or tendon exposure. IPS Index (systolic pressure)> 0.8 with pedal pulses. Wound area less than 300 cm2 surface measurement with Canvas ® software from a photograph of the wound next to which there is a calibration strip. Patients with hypertension. Patient was informed of the study and having signed an informed consent. Exclusion Criteria: Severe distal arteritis (arteritis of large arteries). Histological vasculitis. Collagen (THE BY, scleroderma). Blood Pathology: Cryoglobulinemia, Polycythemia. Hepatitis A, B and C, HIV and syphilis infection Thrombophilia (search for markers during the initial assessment in patients with a history of phlebitis or miscarriage). Hyperthyroidism. Patient treated with Hydrea (favoring the occurrence of ulcers). Patient participating in another study to treat the wound concerned. Topics minors, pregnant women, persons deprived of liberty, adults under legal protection unable to consent.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Anne Dompmartin-Blanchère
Phone
+33 2 31 27 25 09
Email
dompmartin-a@chu-caen.fr
First Name & Middle Initial & Last Name or Official Title & Degree
Marianne Chopinaud
Phone
+33 6 85 82 29 42
Email
mariannechopinaud@hotmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Anne Dompmartin, MD
Organizational Affiliation
University Hospital, Caen
Official's Role
Principal Investigator
Facility Information:
Facility Name
University Hospital, Caen
City
Caen
ZIP/Postal Code
14 000
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Anne Dompmartin
Phone
+33 2 31 27 25 09
Email
dompmartin-a@chu-caen.fr
First Name & Middle Initial & Last Name & Degree
Marianne Chopinaud
Phone
+33 6 85 82 29 42
Email
mariannechopinaud@hotmail.com
First Name & Middle Initial & Last Name & Degree
Anne Dompmartin, MD

12. IPD Sharing Statement

Learn more about this trial

Treatment of Hypertensive Leg Ulcer by Adipose Tissue Grafting

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