Autologous Bone Marrow Mononuclear Cells Transplantation in Treating Diabetes Patients

Phase 1

• Conditions: Diabetes Mellitus, Type 1; Diabetes Mellitus, Type 2

• Registration Number: NCT00465478
• Lead Sponsor: Shandong University

Brief Summary

The study evaluates the safety and efficiency of autologous bone marrow mononuclear cell transplantation in treating patients with type 1 or 2 Diabetes Mellitus. We hypothesize that autologous bone marrow stem cell transplantation will promote β-cells regeneration by directly differentiated from the transplanted BMMCs or stimulated local stem cells regeneration and thus decrease or eliminate the need of exogenous insulin and improve β-cells function.

Detailed Description

Patients with type 1 or 2 Diabetes mellitus will be recruited according to eligibility criteria. Bone marrow mononuclear cells (BMMCs) will be separated from the bone marrow aspirate of each patient and be directly delivered to pancreas via splenic artery with the distal lumen occlusion through an arterial catheter. All patients will be explained in details about the procedures involved in BMMC transplantation and sign the informed consent for the study; The Ethics Committee of Qilu hospital, ShanDong university approved the treatment protocol. All patients undergo scheduled follow-up evaluations for 5 years after transplantation. Clinical, hematological, metabolical evaluations are performed to analyses the effect of the transplant, Patients fitting the inclusion criteria but not agreeing to perform the transplantation are the control group and will received the regular OHA and/or insulin therapy .They are followed in parallel with transplanted patients and will be subjected to the same follow-up management including extensive endocrinological monitoring, diet and exercise program as transplantation patients during the follow-up.

Study Timeline

• Study Start: 2006-03
• Status Verified: 2007-04
• Study First Submitted: 2007-04-24
• Study First Submitted QC: 2007-04-24
• Last Update Submitted: 2007-04-24
• Study First Posted: 2007-04-25
• Last Update Posted: 2007-04-25
• Study Completion: 2014-03

Recruitment & Eligibility

• Status: UNKNOWN
• Sex: All
• Target Recruitment: 200

Inclusion Criteria

• Type 1 or type 2 diabetes
• Between 16 to 65 years of age
• Requiring daily exogenous insulin injection for the glycaemic control
• With poor β-cell function
• Body mass index (BMI) < 28

Exclusion Criteria

• Acute or chronic infections
• Chronic uncompensated organic insufficiency including heart, liver, renal and lung
• Any malignancies, congenital or acquired immunodeficiency
• Hematological diseases or coagulopathy
• Acute or chronic pancreatitis
• History of thoracic or abdominal aorta diseases
• Allergy to iodine
• Pregnancy

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Primary Outcome Measures

Name	Time	Method
Exogenous insulin requirement; Hemoglobin A1C; Glucose and C-peptide level;

Secondary Outcome Measures

Name	Time	Method
Safety assessment parameter: amylase, hepatic function,renal function,
lipid profile, autoantibody， Quality of life

Trial Locations

Locations (1)

Qilu Hospital of Shandong University; 🇨🇳 Jinan, Shandong, China