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Safety and Efficacy of Arterial Delivery of Autologous Bone Marrow Cells in the Treatment of Insulin-Dependent Diabetes

Método Para Regenerar el páncreas Con localización in Vivo de médula ósea Total Autologa en Pacientes diabéticos Tipo 1. Estudio Fase IIB.

Status
Withdrawn
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00971503
Enrollment
34
Registered
2009-09-03
Start date
2011-02-28
Completion date
2012-02-29
Last updated
2011-07-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Type 1 Diabetes Mellitus

Keywords

Diabetes type 1, Adult Stem cells, Local injection, Catheter delivery, Bone marrow

Brief summary

Diabetes mellitus is a long-term multi-organ disease with severe implications that constitute a major health problem worldwide. Type 1 diabetes is an autoimmune disorder in which the body's own immune system attacks and destroys the cells that make insulin. Exogenous administration of insulin is the primary method of controlling type 1 diabetes by regulating blood glucose levels, but this treatment does not reverse nor prevent disease progression. Our hypothesis is that when implanting stimulated total bone marrow by arterial injection directly into the pancreas, we will achieve functional recovery of insulin-producing cells. This study will include patients with chronic type 1 diabetes and absence of lesions in target organs. We will follow the evolution of patients receiving autologous total bone marrow implantation by selective catheterization and compare to a non-treatment control group. All subjects will continue to use insulin therapy as needed to maintain the best possible glucose control. The objective is to achieve a significant increase in C-peptide levels indicating a regeneration of the beta islet cells with a decrease in exogenous insulin usage in at least 70% of the patients. This study is a follow-up to our initial study in which 22 patients received autologous total bone marrow. The initial study was 100% safe but additional studies like the one described above are needed to show efficacy.

Interventions

PROCEDUREautologous bone marrow implantation

Filgrastim treatment before bone marrow aspiration that will then be implanted via pancreatic artery

OTHERSaline injection

Injection of saline solution for 5 days

Sponsors

University of Moron
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 30 Years
Healthy volunteers
No

Inclusion criteria

* Between 18-30 years of age, diagnosed with diabetes mellitus Type 1 (insulin-dependent). * Negative antibody titers for GAD and anti-islet. * Measurements of serum C-peptide below normal values. * BMI 20-25, men, 19-24, women

Exclusion criteria

* Diabetes type 2, gestational diabetes, and other types of secondary diabetes. * Patients with acute metabolic complications of diabetes such as ketoacidosis at least within the last 6 months. * Abdominal perimeter \>102 cm in men; \>88cm in women * Fasting glycemia \>100 mg/dl, triglycerides \>150 mg/dl, HDL \< 40 mg/dl. * Blood pressure: SBP \>135 mmHg and DBP \>85 mmHg at the time of randomization * Patients with BMI \> 25 for men and \>24 for women. * Patients weighing \< 40 kg. * Patients with abnormal ECG indicative of acute or chronic ischemia or acute/chronic necrosis. * Patients with anemias of any origin. * Patients undergoing antibiotic treatment for acute infection. * Patients with any blood abnormality. * Patients with history of moderate to severe pancreatitis. * A female subject who is breast-feeding, pregnant, intends to become pregnant or refuses to use a contraceptive method during the course of the study. * Patients allergic to iodine or filgrastim. * Patients using medications that could affect this study. * Patients with serious mental conditions. * Patients who have undergone a previous stem cell treatment. * Patients who do not accept and sign the informed consent.

Design outcomes

Primary

MeasureTime frame
Significant increase in C-peptide levels after transplant in 70% of the patient.1 month, 3 months, 6 months, 12 months, 18 months, 24 months

Secondary

MeasureTime frame
Reduction by 50% of the insulin requirement after the transplant in 70% of the patients.Two years
Normalization of the hemoglobin A1C after transplant in 70% of the patients. Normalization of blood glucose levels.one year

Countries

Chile

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026