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

Phase 2

Withdrawn

• Conditions: Type 1 Diabetes Mellitus
• Interventions: Procedure: autologous bone marrow implantation; Other: Saline injection

• Registration Number: NCT00971503
• Lead Sponsor: University of Moron

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.

Detailed Description

Not available

Study Timeline

• Study First Submitted: 2009-09-01
• Study First Submitted QC: 2009-09-02
• Study First Posted: 2009-09-03
• Study Start: 2011-02
• Primary Completion: 2011-02
• Status Verified: 2011-07
• Last Update Submitted: 2011-07-26
• Last Update Posted: 2011-07-27
• Study Completion: 2012-02

Recruitment & Eligibility

• Status: WITHDRAWN
• Sex: All
• Target Recruitment: 34

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.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Autologous bone marrow implantation	autologous bone marrow implantation	-
saline injection	Saline injection	-

Primary Outcome Measures

Name	Time	Method
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 Outcome Measures

Name	Time	Method
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

Trial Locations

Locations (1)

School of Medicine, Pontificia Universidad Catolica de Chile; 🇨🇱 Santiago de Chile, Chile