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Clinical Trial I/II Opened, Randomized and Controlled for the Study of the Use of Stem Cells Therapy in Insulinized Diabetic Patients Type 2 With Critical Ischemia in Lower Limbs (CLI): Study of the Needs of Insulin

Primary Purpose

Critical Limb Ischemia (CLI)

Status
Terminated
Phase
Phase 1
Locations
Spain
Study Type
Interventional
Intervention
Stem cell infusion
Sponsored by
Andalusian Initiative for Advanced Therapies - Fundación Pública Andaluza Progreso y Salud
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Critical Limb Ischemia (CLI)

Eligibility Criteria

18 Years - 85 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Age ≥18 and ≤ 85 years
  2. Diabetic type 2, in treatment with insulin at least 3 previous months.
  3. Vascular disease infrapopliteal atherosclerotic of severe degree (Patients with category Rutherford-Becker ≥ 4), pretty or bilateral. The critical ischemia of the foot is defined as a persistent / persistent pain that needs analgesia and / or not healing present sores> 4 weeks, without evidence of improvement with conventional therapies and / or walking test between 1-6 minutes in two ergometries separated at least for 2 weeks and / or index ankle - arm in rest <0,8.
  4. Impossibility of revascularization surgical or endovascular or I fail in the surgery of revascularization performed at least 30 days before, with persistence or entry in phase of critical ischemia
  5. Life expectancy > 2 years.
  6. Major amputation is not foreseen in any of the members in the next 6 months after the incorporation.
  7. Normal Biochemical and bone marrow parameters defined for:

    • Leukocytes ≥ 3000
    • Neutrophils ≥ 1500
    • Platelets ≥ 140000
    • AST/ALT ≤ 2,5 standard range institution
    • Creatinine ≤2,5 mg/dl and explanation of creatinine ≤ 30 ml/min (MDRD4)
  8. The women in fertile age will have to obtain negative results in a pregnancy test realized in the moment of the incorporation in the study and promise to use a contraceptive method medically approved while the study lasts.
  9. Patients who give his Informed Consent in writing for the participation in the study. 10. Patients who have not taken part in another clinical trial in the last 3 months before the incorporation.

Exclusion Criteria:

  1. Precedent of neoplasia or hematologic disease (disease myeloproliferative, syndrome myelodysplasic or leukaemia) in the last 2 years.
  2. Major previous amputation.
  3. Patients with arterial uncontrolled hypertension (defined as arterial tension> 180/110 in more than one occasion).
  4. Cardiac severe insufficiency (NYHA the IVth) or Fraction of Ejection of left ventricle (FAITH) lower than 30 %.
  5. Patients with ventricular malignant arrhythmias or unstable angina.
  6. Diagnosis of venous deep thrombosis in 3 previous months.
  7. Patients with genotype DD of the ECA or genotype E4 of the apo E.
  8. Concomitant therapy that includes oxygen hyperbaric, vasoactive substances, agents against angiogenesis or inhibiting Cox-II. The agents use is allowed antiplatelets.
  9. Index of corporal mass> 40 Kg/m2.
  10. Patients with the diagnosis of alcoholism in the moment of the incorporation.
  11. Proliferative Retinopathy without possibility of treatment.
  12. Diabetic Nephropathy with haemodialysis
  13. Concomitant disease that reduces the life expectancy to less than 1 years.
  14. Impossibility foreseen to obtain the inhaled one of 100ml of bone marrow.
  15. Infection for HIV, Hepatitis B or Hepatitis C.
  16. Impede in the follow-up.
  17. ACV or heart attack of myocardium in the last 3 months
  18. Anaemia (Haemoglobin <7.9 g/dl)
  19. Patients before treated with cellular therapy.

Sites / Locations

  • Hopsital U. Virgen Macarena
  • CABIMER (Andalusian Center for Molecular Biology and Regenerative Medicine)

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

Experimental

Experimental

Active Comparator

Arm Label

Autologous mononuclear stem cell from the bone marrow

Autologous endothelial stem cell from the bone marrow

Autologous mesenchymal stem cells from the adiposite tissue

Current medication for the disease

Arm Description

Autologous mononuclear stem cell from the bone marrow in an unique infusion of 150-250 millions of cells

Autologous endothelial progenitor CD133 stem cell from the bone marrow in an unique infusion of 2 - 7 millions of CD133 cells

Autologous mesenchymal stem cells from the adipose tissue in an unique infusion of 0.5 millions of cells

Current medication for the disease

Outcomes

Primary Outcome Measures

Serious Adverse Events
To evaluate the possible complications derived from the procedure (in the first 24 hours after the infusion of stem cells and the incident of Serious Adverse Events and not Serious Adverse Events related to the IMPD or to the procedure of administration

Secondary Outcome Measures

Efficacy measured by: The changes in the requirements of insulin, Peptide C, Resistance to the insulin, inflammatory Cytokines, pancreatic Reservation, Quantification of the degree of neovascularization (angio/arteriogenesis and vasculogenesis)
Efficacy measured by: The changes in the requirements of insulin, Peptide C, Resistance to the insulin, inflammatory Cytokines, pancreatic Reservation, Quantification of the degree of neovascularization (angio/arteriogenesis and vasculogenesis) after 6 months of the stem cells infusion

Full Information

First Posted
February 25, 2013
Last Updated
December 17, 2018
Sponsor
Andalusian Initiative for Advanced Therapies - Fundación Pública Andaluza Progreso y Salud
Collaborators
Iniciativa Andaluza en Terapias Avanzadas
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1. Study Identification

Unique Protocol Identification Number
NCT02287974
Brief Title
Clinical Trial I/II Opened, Randomized and Controlled for the Study of the Use of Stem Cells Therapy in Insulinized Diabetic Patients Type 2 With Critical Ischemia in Lower Limbs (CLI): Study of the Needs of Insulin
Official Title
Clinical Trial I/II Opened, Randomized and Controlled for the Study of the Use of Stem Cells Therapy in Insulinized Diabetic Patients Type 2 With Critical Ischemia in Lower Limbs: Study of the Needs of Insulin
Study Type
Interventional

2. Study Status

Record Verification Date
July 2018
Overall Recruitment Status
Terminated
Why Stopped
Patients' numebr randomized not achieved. Investigators team with lack of interest and commitment. The sponsor closed prematurely patients' recruitment.
Study Start Date
September 2011 (undefined)
Primary Completion Date
July 2018 (Actual)
Study Completion Date
July 2018 (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
No

5. Study Description

Brief Summary
To study the effect of the stem cells therapy autologous mononuclear from the bone marrow, autologous progenitor endothelial CD133 cells from the bone marrow and autologous mesenchymal stem cells from adipose tissue on the inflammatory cytokines, the resistance to insulin and the decrease of the needs of insulin, besides evaluates the safety, viability and efficiency of the intra-arterial infusion of stem cells in diabetic patients type 2 with CLI.
Detailed Description
To study the effect of the stem cells therapy autologous mononuclear from the bone marrow, autologous progenitor endothelial CD133 cells from the bone marrow and autologous mesenchymal stem cells from adipose tissue on the inflammatory cytokines, the resistance to insulin and the decrease of the needs of insulin, besides evaluates the safety, viability and efficiency of the intra-arterial infusion of stem cells in diabetic patients type 2. Diabetic patients will include with critical ischemia chronicle of at least a low member limb (CLI) and without possibilities of revascularization. 48 evaluable patients will be included, of which 36 patients will be included in the experimental group (12 for every cellular group) and 12 in the group control by conventional treatment. The population to studying will be constituted by 48 evaluable patients.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Critical Limb Ischemia (CLI)

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1, Phase 2
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
20 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Autologous mononuclear stem cell from the bone marrow
Arm Type
Experimental
Arm Description
Autologous mononuclear stem cell from the bone marrow in an unique infusion of 150-250 millions of cells
Arm Title
Autologous endothelial stem cell from the bone marrow
Arm Type
Experimental
Arm Description
Autologous endothelial progenitor CD133 stem cell from the bone marrow in an unique infusion of 2 - 7 millions of CD133 cells
Arm Title
Autologous mesenchymal stem cells from the adiposite tissue
Arm Type
Experimental
Arm Description
Autologous mesenchymal stem cells from the adipose tissue in an unique infusion of 0.5 millions of cells
Arm Title
Current medication for the disease
Arm Type
Active Comparator
Arm Description
Current medication for the disease
Intervention Type
Drug
Intervention Name(s)
Stem cell infusion
Intervention Description
Unique stem cell infusion of the randomized group
Primary Outcome Measure Information:
Title
Serious Adverse Events
Description
To evaluate the possible complications derived from the procedure (in the first 24 hours after the infusion of stem cells and the incident of Serious Adverse Events and not Serious Adverse Events related to the IMPD or to the procedure of administration
Time Frame
the entire follow-up period, in the first 24 hours after the infusion of stem cells
Secondary Outcome Measure Information:
Title
Efficacy measured by: The changes in the requirements of insulin, Peptide C, Resistance to the insulin, inflammatory Cytokines, pancreatic Reservation, Quantification of the degree of neovascularization (angio/arteriogenesis and vasculogenesis)
Description
Efficacy measured by: The changes in the requirements of insulin, Peptide C, Resistance to the insulin, inflammatory Cytokines, pancreatic Reservation, Quantification of the degree of neovascularization (angio/arteriogenesis and vasculogenesis) after 6 months of the stem cells infusion
Time Frame
6 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: Age ≥18 and ≤ 85 years Diabetic type 2, in treatment with insulin at least 3 previous months. Vascular disease infrapopliteal atherosclerotic of severe degree (Patients with category Rutherford-Becker ≥ 4), pretty or bilateral. The critical ischemia of the foot is defined as a persistent / persistent pain that needs analgesia and / or not healing present sores> 4 weeks, without evidence of improvement with conventional therapies and / or walking test between 1-6 minutes in two ergometries separated at least for 2 weeks and / or index ankle - arm in rest <0,8. Impossibility of revascularization surgical or endovascular or I fail in the surgery of revascularization performed at least 30 days before, with persistence or entry in phase of critical ischemia Life expectancy > 2 years. Major amputation is not foreseen in any of the members in the next 6 months after the incorporation. Normal Biochemical and bone marrow parameters defined for: Leukocytes ≥ 3000 Neutrophils ≥ 1500 Platelets ≥ 140000 AST/ALT ≤ 2,5 standard range institution Creatinine ≤2,5 mg/dl and explanation of creatinine ≤ 30 ml/min (MDRD4) The women in fertile age will have to obtain negative results in a pregnancy test realized in the moment of the incorporation in the study and promise to use a contraceptive method medically approved while the study lasts. Patients who give his Informed Consent in writing for the participation in the study. 10. Patients who have not taken part in another clinical trial in the last 3 months before the incorporation. Exclusion Criteria: Precedent of neoplasia or hematologic disease (disease myeloproliferative, syndrome myelodysplasic or leukaemia) in the last 2 years. Major previous amputation. Patients with arterial uncontrolled hypertension (defined as arterial tension> 180/110 in more than one occasion). Cardiac severe insufficiency (NYHA the IVth) or Fraction of Ejection of left ventricle (FAITH) lower than 30 %. Patients with ventricular malignant arrhythmias or unstable angina. Diagnosis of venous deep thrombosis in 3 previous months. Patients with genotype DD of the ECA or genotype E4 of the apo E. Concomitant therapy that includes oxygen hyperbaric, vasoactive substances, agents against angiogenesis or inhibiting Cox-II. The agents use is allowed antiplatelets. Index of corporal mass> 40 Kg/m2. Patients with the diagnosis of alcoholism in the moment of the incorporation. Proliferative Retinopathy without possibility of treatment. Diabetic Nephropathy with haemodialysis Concomitant disease that reduces the life expectancy to less than 1 years. Impossibility foreseen to obtain the inhaled one of 100ml of bone marrow. Infection for HIV, Hepatitis B or Hepatitis C. Impede in the follow-up. ACV or heart attack of myocardium in the last 3 months Anaemia (Haemoglobin <7.9 g/dl) Patients before treated with cellular therapy.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Bernat Soria
Organizational Affiliation
CABIMER (Centro Andaluz de Biología Molecular y Medicina Regenerativa)
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hopsital U. Virgen Macarena
City
Sevilla
State/Province
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

Clinical Trial I/II Opened, Randomized and Controlled for the Study of the Use of Stem Cells Therapy in Insulinized Diabetic Patients Type 2 With Critical Ischemia in Lower Limbs (CLI): Study of the Needs of Insulin

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