Bone Marrow Mononuclear Cells vs Mesenchymal Stem Cells in Diabetic Patients With Chronic Limb Ischemia

Fundación Oftalmológica de Santander Clínica Carlos Ardila Lulle

Status and phase: Completed; Phase 2; Phase 1

Conditions: Chronic Limb-threatening Ischemia; Diabetes Mellitus

Treatments: Biological: Cell-based therapy

Study type: Interventional

Funder types: Other

Identifiers

NCT05631444

CLTI 01

Details and patient eligibility

About

Patients in the severe stages of Chronic limb-threatening ischemia (CLTI) are prone to amputation and death, leading to poor quality of life and a great socioeconomic burden.

There is an urgent need to develop an effective therapeutic strategy to treat this disease. In this context, autologous bone marrow mononuclear cells (BM-MNC) and allogeneic mesenchymal stem cells derived from different sources have emerged as promising therapeutic approaches for this condition.

Full description

Comparison of the therapeutic potential of BM-MNC vs. allogeneic Wharton jelly-derived mesenchymal stem cells (allo-WJ-MSCs) in diabetic patients with CLTI.

Twenty-four type 2 diabetic patients in the most severe stages of the CLTI (category 4 or 5 in Rutherford's classification and transcutaneous oxygen pressure (TcPO2) below 30 mm Hg were enrolled and randomized to receive 15 injections of (i) BM-MNC (7.197x106 ± 2.984 x106 cells/mL each with 2% of autologous serum) (n=7), (ii) allo-WJ-MSCs (1.333 x106 cells/mL each with 5% of human serum albumin serum) (n=7) or (iii) placebo solution (1 mL saline solution with 2% of autologous serum) (n=10), which were administered into the periadventitial arteries.

The follow-up visits were at months 1, 3, 6, and 12, to evaluate the following parameters:

(i) Rutherford classification (0 to 6) (ii) TcPO2 (mmHg) (iii) Wound closure (area cm2) (iv) pain (visual analogue scale (0-10) (v) pain-free walking distance (m) (vi) revascularization and limb-survival proportion during follow-up (vii) the quality of life (EQ-5D questionnaire).

Enrollment: 24 patients

Sex: All

Ages: 40 to 85 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Adult male or female, 40 years of age or over (until 85 years old)
• TcPO2 ≤ 30 mmHg.
• Diagnosis of diabetes.
• Patients with signs of critical ischemia such as (i) ulcer that does not heal, (ii) necrosis or loss of tissue, (iii) pain at rest, and (iv) intermittent claudication.
• Basal Rutherford classification stage 3 to 5.
• Non-revascularizable patients due to comorbidities and/or anatomy.
• Patients that despite revascularization (vascular surgery), have adequate distal beds to perfuse the limb.
• Ankle/brachial index less than 0.4.
• Stenosis or occlusion of the infrapatellar arteries.

Exclusion criteria

• Participants that do not sign the informed consent.
• Presence of osteomyelitis.
• Hemodynamic instability (MAP<65 mmHg or vasopressor requirement).
• Any acute systemic infectious disease process.
• Severe sepsis.
• Uncontrolled coagulopathy.
• Condition of cancer.
• Use of immunosuppressive or cytotoxic drugs
• Alterations of the bone marrow that do not allow the adequate extraction of the components to be used as: acute leukemia, chronic leukemia, marrow aplasia, myelodysplastic syndrome, and myelophthisis.
• Contraindication of sedation for bone marrow aspirate.
• Patients who have suffered in a period < six months of myocardial infarction, disease cerebrovascular or coronary intervention.
• Patients with liver failure indicated by serum transaminases (aspartate aminotransferase and alanine aminotransferase), with values twice the normal limit.
• Any acute or chronic contagious disease including hepatitis B, hepatitis C, and HIV.
• Any other comorbidity that the treating vascular surgeon considers as a contraindication to cell treatments.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Triple Blind

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24 participants in 3 patient groups, including a placebo group

Placebo group

Placebo Comparator group

Description:

Placebo group (n=10), which consisted of 15 injections of 1 mL of vehicle (1 mL saline solution with 2% of autologous serum) on periadventitial arteries in one dose at day 0.

Treatment:

Biological: Cell-based therapy

Auto-BM-MNC

Experimental group

Description:

Auto-BM-MNC (n=7) were obtained from diabetic patients. Fifteen injections of 7.197x106 ± 2.984x106 cells/mL each with 2% of autologous serum were periadventitial arteries administrated in one dose at day 0.

Treatment:

Biological: Cell-based therapy

Allo-WJ-MSCs

Experimental group

Description:

Allo-WJ-MSCs (n=7) were obtained from culturing the WJ from healthy cordon umbilical donors unrelated to the patient. Fifteen injections of 1.333x106 cells/mL each with 5% of human serum albumin serum were periadventitial arteries administrated in one dose at day 0.

Treatment:

Biological: Cell-based therapy