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The Effect of Treatment With Umbilical Cord Blood Platelet Lysate on Diabetic Foot Ulcers

Primary Purpose

Diabetic Foot

Status
Recruiting
Phase
Phase 4
Locations
Greece
Study Type
Interventional
Intervention
Umbilical cord blood platelel lysate gel
Sponsored by
Attikon Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Diabetic Foot

Eligibility Criteria

18 Years - 95 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • age>18 years old
  • patients with diabetic foot ulcer, foot ulcer located on the plantar, medial, or lateral aspect of the foot (including all toe surfaces)
  • ulcer with area(length x width) measurement<30 cm2
  • non-infected ulcers

Exclusion Criteria:

  • pregnacy
  • venous ulcers
  • clinical signs and symptoms of infection
  • exposure of bone, muscle, ligaments, or tendons and the presence of tunneling

Sites / Locations

  • Catherine Stavropoulos-GiokasRecruiting
  • Vaia LambadiariRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

Umbilical cord blood platelel lysate group

Control group

Arm Description

A Umbilical cord blood platelel lysate gel will be applied in diabetic foot ulcer every three days for one month.

The control group will receive the clinical standard of care; removable of any necrotic, hyperkeratotic and infected tissue, cleansing of the wound with normal saline and covering of the ulcer with dressing with normal saline and then with a few layers of sterile gauze, and non-compressible bandage.

Outcomes

Primary Outcome Measures

The efficacy of UCB-PL in ulcer healing by assessing the change in ulcer size.
Primary endpoint was to investigate the efficacy of UCB-PL in ulcer healing by assessing the change in ulcer size over the six months follow-up by using the imito-measure application.

Secondary Outcome Measures

Full Information

First Posted
May 31, 2022
Last Updated
February 7, 2023
Sponsor
Attikon Hospital
Collaborators
Biomedical Research Foundation, Academy of Athens
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1. Study Identification

Unique Protocol Identification Number
NCT05404295
Brief Title
The Effect of Treatment With Umbilical Cord Blood Platelet Lysate on Diabetic Foot Ulcers
Official Title
The Effect of Treatment With Umbilical Cord Blood Platelet Lysate on Diabetic Foot Ulcers:a Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
February 2023
Overall Recruitment Status
Recruiting
Study Start Date
June 10, 2019 (Actual)
Primary Completion Date
June 10, 2022 (Actual)
Study Completion Date
April 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Attikon Hospital
Collaborators
Biomedical Research Foundation, Academy of Athens

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
Application of autologous Platelet Rich Plasma (PRP) has been a major breakthrough for the treatment of diabetic foot ulcers, as it provides the necessary growth factors which enhance tissue healing. Human umbilical cord blood platelet lysate (UCB-PL) contains a supraphysiological concentration of growth factors. The aim of the study is to evaluate the efficacy of umbilical cord blood platelet lysate (UCB-PL) gel for the treatment of diabetic foot ulcer.
Detailed Description
110 patients with diabetic foot ulcer will be randomized to receive UCB-PL gel or regular dressing with normal saline. The diabetic foot ulcers will be first debrided to remove any necrotic and infected tissues or hyperkeratotic skin. Afterward, the wound area will be cleaned thoroughly with normal saline. Ulcer length, width and surface will be measured before any study procedure. The UCB-PL gel in the treatment group and the dressing with normal saline in the control group will be applied in the ulcer, and then a few layers of sterile gauze, and non-compressible bandage will be used to cover the wound/ulcer area. This will be repeated every three days for one month. After the fist one month of treatment, the patients will be followed up for a period of 20 weeks post-treatment. Care and management efforts will be provided at each visit included cleansing and assessing of the wound, obtaining an interim wound history, including information regarding adverse events, concomitant medications and other aspects of care since the last visit. Ulcers will be photographed at two weeks, at four weeks, at two months, at four months and at six months.

6. Conditions and Keywords

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

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Sequential Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
120 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Umbilical cord blood platelel lysate group
Arm Type
Active Comparator
Arm Description
A Umbilical cord blood platelel lysate gel will be applied in diabetic foot ulcer every three days for one month.
Arm Title
Control group
Arm Type
Placebo Comparator
Arm Description
The control group will receive the clinical standard of care; removable of any necrotic, hyperkeratotic and infected tissue, cleansing of the wound with normal saline and covering of the ulcer with dressing with normal saline and then with a few layers of sterile gauze, and non-compressible bandage.
Intervention Type
Other
Intervention Name(s)
Umbilical cord blood platelel lysate gel
Intervention Description
For the treatment group, a gel from Umbilical cord blood platelel lysat will be applied in the ulcer, and then a few layers of sterile gauze, and non-compressible bandage will be used to cover the wound/ulcer area.
Primary Outcome Measure Information:
Title
The efficacy of UCB-PL in ulcer healing by assessing the change in ulcer size.
Description
Primary endpoint was to investigate the efficacy of UCB-PL in ulcer healing by assessing the change in ulcer size over the six months follow-up by using the imito-measure application.
Time Frame
six months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
95 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: age>18 years old patients with diabetic foot ulcer, foot ulcer located on the plantar, medial, or lateral aspect of the foot (including all toe surfaces) ulcer with area(length x width) measurement<30 cm2 non-infected ulcers Exclusion Criteria: pregnacy venous ulcers clinical signs and symptoms of infection exposure of bone, muscle, ligaments, or tendons and the presence of tunneling
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Vaia Lambadiari, Professor
Phone
2105831148
Email
vlambad@otenet.gr
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Vaia Lambadiari, Professor
Organizational Affiliation
General University Attikon Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Catherine Stavropoulos-Giokas
City
Athens
State/Province
Attiki
ZIP/Postal Code
11527
Country
Greece
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Catherine Stavropoulos-Giokas
Phone
21 06597342
Email
cstavrop@bioacademy.gr
Facility Name
Vaia Lambadiari
City
Athens
State/Province
Attiki
ZIP/Postal Code
12462
Country
Greece
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Vaia Lambadiari, Professor
Phone
2105831148
Email
vlambad@otenet.gr

12. IPD Sharing Statement

Learn more about this trial

The Effect of Treatment With Umbilical Cord Blood Platelet Lysate on Diabetic Foot Ulcers

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