Human Adipose Derived Mesenchymal Stem Cells for Critical Limb Ischemia (CLI) in Diabetic Patients
Primary Purpose
Critical Limb Ischemia (CLI), Diabetes
Status
Completed
Phase
Phase 1
Locations
Spain
Study Type
Interventional
Intervention
Autologous adipose derived mesenchymal stem cells
Sponsored by

About this trial
This is an interventional treatment trial for Critical Limb Ischemia (CLI) focused on measuring Critical Limb Ischemia (CLI), Diabetes, Mesenchymal Stem Cells, Regenerative Therapy
Eligibility Criteria
Inclusion Criteria:
- Diabetes, type 1 or 2
- Critical Limb Ischemia (Rutherford Becker Class II,III or IV)of at least one limb.
- No options for target limb revascularization.
Exclusion Criteria:
- Cancer antecedent in the last two years
- Current limb infection or limb gangrene
Sites / Locations
- University Hospital Virgen Macarena
- CABIMER (Andalusian Center for Molecular Biology and Regenerative Medicine)
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Active Comparator
Active Comparator
No Intervention
Arm Label
Mesenchymal stem cells 0,5 million * weight (kg)
Mesenchymal stem cells 1 million * weight (kg)
Controlled group
Arm Description
Group of low dose of Mesenchymal stem cells.
Group of mid dose of mesenchymal stem cells
Controlled group with no intervention
Outcomes
Primary Outcome Measures
Angiographic assessment of neovasculogenesis (angiogenesis plus arteriogenesis)
Target limb vascularization would be quantified by a dedicated software, MetaMorph® v.6.3, by using Angiogenesis Tube Formation application module. Neovasculogenesis would be the difference between vascularization at baseline and 6 months follow-up.
Major adverse event (death, target limb amputation)
Secondary Outcome Measures
Ankle Brachial Index
University of Texas Classification at target limb
Full Information
NCT ID
NCT01257776
First Posted
December 9, 2010
Last Updated
August 4, 2015
Sponsor
Andalusian Initiative for Advanced Therapies - Fundación Pública Andaluza Progreso y Salud
Collaborators
Iniciativa Andaluza en Terapias Avanzadas
1. Study Identification
Unique Protocol Identification Number
NCT01257776
Brief Title
Human Adipose Derived Mesenchymal Stem Cells for Critical Limb Ischemia (CLI) in Diabetic Patients
Official Title
Using Mesenchymal Stem Cells From Adipose Tissue (CeTMAd) as Cell Regeneration Therapy in Chronic Ischemic Syndrome of Lower Limbs in Diabetic Patients
Study Type
Interventional
2. Study Status
Record Verification Date
November 2014
Overall Recruitment Status
Completed
Study Start Date
December 2010 (undefined)
Primary Completion Date
February 2013 (Actual)
Study Completion Date
July 2015 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Andalusian Initiative for Advanced Therapies - Fundación Pública Andaluza Progreso y Salud
Collaborators
Iniciativa Andaluza en Terapias Avanzadas
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
A prospective, multicenter, open, randomized, parallel-group controlled study for two levels of dose.
The study population will consist of 30 non-diabetic patients with critical chronic ischemia in at least one of the lower limbs (CLI) and without possibility of revascularization, from whom results can clinically be evaluable, of whom, 20 patients will be included in the experimental group (10 for each dose level) and 10 in the control group.
In each of the two dose levels to be used in the study, 15 patients will be included, who will be randomized to the experimental group or the control group according to a distribution 2:1 (2 patients in the experimental group and 1 in control group), thus at each dose level, we will have 10 patients in the experimental group (treated with mesenchymal cells of adipose tissue) and 5 patients in the control group (conventional treatment)
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Critical Limb Ischemia (CLI), Diabetes
Keywords
Critical Limb Ischemia (CLI), Diabetes, Mesenchymal Stem Cells, Regenerative Therapy
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 1, Phase 2
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
33 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Mesenchymal stem cells 0,5 million * weight (kg)
Arm Type
Active Comparator
Arm Description
Group of low dose of Mesenchymal stem cells.
Arm Title
Mesenchymal stem cells 1 million * weight (kg)
Arm Type
Active Comparator
Arm Description
Group of mid dose of mesenchymal stem cells
Arm Title
Controlled group
Arm Type
No Intervention
Arm Description
Controlled group with no intervention
Intervention Type
Drug
Intervention Name(s)
Autologous adipose derived mesenchymal stem cells
Intervention Description
Intra-arterial administration through a selective cannulation of target common femoral artery
Primary Outcome Measure Information:
Title
Angiographic assessment of neovasculogenesis (angiogenesis plus arteriogenesis)
Description
Target limb vascularization would be quantified by a dedicated software, MetaMorph® v.6.3, by using Angiogenesis Tube Formation application module. Neovasculogenesis would be the difference between vascularization at baseline and 6 months follow-up.
Time Frame
6 months
Title
Major adverse event (death, target limb amputation)
Time Frame
1 month, 6 months, 12 months
Secondary Outcome Measure Information:
Title
Ankle Brachial Index
Time Frame
1 month, 6 months, 12 months
Title
University of Texas Classification at target limb
Time Frame
1 month, 6 months, 12 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Diabetes, type 1 or 2
Critical Limb Ischemia (Rutherford Becker Class II,III or IV)of at least one limb.
No options for target limb revascularization.
Exclusion Criteria:
Cancer antecedent in the last two years
Current limb infection or limb gangrene
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Rafael J Ruiz-Salmeron, MD, PhD
Organizational Affiliation
University Hospital Virgen Macarena. Seville.Spain
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Antonio De la Cuesta, MD
Organizational Affiliation
University Hospital Virgen Macarena. Seville.Spain
Official's Role
Principal Investigator
Facility Information:
Facility Name
University Hospital Virgen Macarena
City
Seville
ZIP/Postal Code
41007
Country
Spain
Facility Name
CABIMER (Andalusian Center for Molecular Biology and Regenerative Medicine)
City
Seville
ZIP/Postal Code
41092
Country
Spain
12. IPD Sharing Statement
Learn more about this trial
Human Adipose Derived Mesenchymal Stem Cells for Critical Limb Ischemia (CLI) in Diabetic Patients
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