Mesenchymal Stromal Cell Derivatives in the Treatment of Chronic Diabetic Foot Ulcers Type 1 and 2 (MSCDTDFU)
Primary Purpose
Foot Ulcer, Diabetic
Status
Unknown status
Phase
Phase 1
Locations
Study Type
Interventional
Intervention
dac-MSCs
MSCs
Fitostimoline
Sponsored by
About this trial
This is an interventional treatment trial for Foot Ulcer, Diabetic focused on measuring Mesenchymal stromal cells, Fitostimoline, MSC derivatives, Diabetes
Eligibility Criteria
Inclusion Criteria:
- Males and females between the ages of 40 and 80 years, inclusive, with Type 1 or 2 diabetes as defined by the American Diabetes Association
- Stable glycemic control
- Transcutaneous oxygen measurement > 30 mmHg
- Ulcer present at least for 1 month
- Wound size between 0.5 and 5 cm2
- Subjects that require endovascular surgical intervention
- Subjects must have adequate nutrition (albumin level > 2 g/dL and prealbumin level > 15 mg/dL)
Exclusion Criteria:
- Previous or current diagnoses with one of the following: cancer, symptomatic coronary artery disease, brain disease, kidney failure, blood disorders
- Taking immunosuppressive and cytotoxic drugs
- Presence of active systemic infection
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Experimental
Active Comparator
Active Comparator
Arm Label
dac-MSCs and Fitostimoline
MSCs and Fitostimoline
Fitostimoline
Arm Description
Intradermic application of dac-MSCs (1 mL ) in four equidistant points around the ulcer (twice: day 0 and 7) and topical application of fitostimoline every other day
Intradermic application of MSCs (500,000 cells/mL) in four equidistant points around the ulcer (once: day 0 ) and topical application of fitostimoline every other day
Topical application of fitostimoline every other day
Outcomes
Primary Outcome Measures
Wound size change
Wound size will be assessed using a SilhouetteMobile camera (digital planimetry)
Secondary Outcome Measures
Granulation tissue percentage
Images will be used to assess the amount of granulation tissue present in the wound
Pigmentation change
Digital images will be used to evaluate color changes in the wound
Presence of Exudate
Visual observation of the wound to determine the presence of exudate
Full Information
NCT ID
NCT02943486
First Posted
October 19, 2016
Last Updated
October 21, 2016
Sponsor
Universidad Autónoma de Bucaramanga
Collaborators
Fundación Oftalmológica de Santander Clínica Carlos Ardila Lulle, Instituto Colombiano para el Desarrollo de la Ciencia y la Tecnología (COLCIENCIAS)
1. Study Identification
Unique Protocol Identification Number
NCT02943486
Brief Title
Mesenchymal Stromal Cell Derivatives in the Treatment of Chronic Diabetic Foot Ulcers Type 1 and 2
Acronym
MSCDTDFU
Official Title
Mesenchymal Stromal Cell Derivatives: a New Alternative and Potential Product for the Treatment of Diabetic Foot Ulcers 1 and 2
Study Type
Interventional
2. Study Status
Record Verification Date
October 2016
Overall Recruitment Status
Unknown status
Study Start Date
January 2017 (undefined)
Primary Completion Date
June 2018 (Anticipated)
Study Completion Date
January 2019 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Universidad Autónoma de Bucaramanga
Collaborators
Fundación Oftalmológica de Santander Clínica Carlos Ardila Lulle, Instituto Colombiano para el Desarrollo de la Ciencia y la Tecnología (COLCIENCIAS)
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The goal of this study is to evaluate the safety and efficacy of using mesenchymal stromal cell derivatives (dac-MSCs) in the treatment of chronic diabetic foot ulcers (type 1 and 2) in adults. A third of the participants will receive dac-MSCs and Triticum vulgare (Fitostimoline) in combination, the other third MSCs and Fitostimoline in combination, and the last third only Fitosimoline. This study will be a randomized, blind, and parallel and controlled-group trial.
Detailed Description
Conventional treatments such as dry, wet or active dressings are effective only in 50% of patients with diabetic foot ulcer. The remaining 50% of patients have non-responding recoveries that leads to amputation of the compromised limbs. Currently, the administration of mesenchymal stem cells (MSCs) in animal models or in small groups of patients with diabetic foot ulcer has shown to be safe and effective. Particularly, the use of these cells induce regeneration, both in the dermis and the epidermis. Nevertheless, MSC transplantation has some limitations, for instance, time restrictions in the availability of cells due to their isolation and expansion as well as the complex and costly large-scale production. In the same manner, the cryopreservation might cause deleterious effects that affect the biological activity of the cells and a medical professional should conduct the cell administration. In addition, different studies report variability in the results due to the inconsistency in the methods that they used (extraction protocols, cultivation, expansion and administration). The investigators' recent studies in mice with skin lesions, particularly type 1 diabetes, have shown that the presence of the cells is not necessary to promote skin regeneration and the administration of dac-MSCs is sufficient to stimulate would healing.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Foot Ulcer, Diabetic
Keywords
Mesenchymal stromal cells, Fitostimoline, MSC derivatives, Diabetes
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 1, Phase 2
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
51 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
dac-MSCs and Fitostimoline
Arm Type
Experimental
Arm Description
Intradermic application of dac-MSCs (1 mL ) in four equidistant points around the ulcer (twice: day 0 and 7) and topical application of fitostimoline every other day
Arm Title
MSCs and Fitostimoline
Arm Type
Active Comparator
Arm Description
Intradermic application of MSCs (500,000 cells/mL) in four equidistant points around the ulcer (once: day 0 ) and topical application of fitostimoline every other day
Arm Title
Fitostimoline
Arm Type
Active Comparator
Arm Description
Topical application of fitostimoline every other day
Intervention Type
Other
Intervention Name(s)
dac-MSCs
Other Intervention Name(s)
Cell-free therapy
Intervention Description
Cell-free therapy
Intervention Type
Other
Intervention Name(s)
MSCs
Other Intervention Name(s)
Cell-based therapy
Intervention Description
Cell-based therapy
Intervention Type
Drug
Intervention Name(s)
Fitostimoline
Other Intervention Name(s)
Triticum vulgare
Intervention Description
Triticum vulgare
Primary Outcome Measure Information:
Title
Wound size change
Description
Wound size will be assessed using a SilhouetteMobile camera (digital planimetry)
Time Frame
One year
Secondary Outcome Measure Information:
Title
Granulation tissue percentage
Description
Images will be used to assess the amount of granulation tissue present in the wound
Time Frame
One year
Title
Pigmentation change
Description
Digital images will be used to evaluate color changes in the wound
Time Frame
One year
Title
Presence of Exudate
Description
Visual observation of the wound to determine the presence of exudate
Time Frame
One year
10. Eligibility
Sex
All
Minimum Age & Unit of Time
40 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Males and females between the ages of 40 and 80 years, inclusive, with Type 1 or 2 diabetes as defined by the American Diabetes Association
Stable glycemic control
Transcutaneous oxygen measurement > 30 mmHg
Ulcer present at least for 1 month
Wound size between 0.5 and 5 cm2
Subjects that require endovascular surgical intervention
Subjects must have adequate nutrition (albumin level > 2 g/dL and prealbumin level > 15 mg/dL)
Exclusion Criteria:
Previous or current diagnoses with one of the following: cancer, symptomatic coronary artery disease, brain disease, kidney failure, blood disorders
Taking immunosuppressive and cytotoxic drugs
Presence of active systemic infection
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Claudia L Sossa-Melo, MD
Phone
+57 7 643 6261
Ext
587
Email
claudiasossa@gmail.com
First Name & Middle Initial & Last Name or Official Title & Degree
Martha L Arango-Rodríguez, Ph.D.
Phone
+57 679 7979
Ext
6086
Email
martha.arango@fosunab.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Claudia L Sossa-Melo, MD
Organizational Affiliation
Universidad Autónoma de Bucaramanga
Official's Role
Principal Investigator
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Mesenchymal Stromal Cell Derivatives in the Treatment of Chronic Diabetic Foot Ulcers Type 1 and 2
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