Autologous Bone Marrow Mononuclear Cell Transplantation in Treating Type 2 Diabetes Mellitus

NCT01677013 · Status: COMPLETED · Phase: PHASE1/PHASE2 · Type: INTERVENTIONAL · Enrollment: 1026

Last updated 2017-10-03

No results posted yet for this study

Summary

The study is aimed to evaluate the safety and efficiency of autologous bone marrow mononuclear cell transplantation in treating selective patients with type 2 Diabetes Mellitus. We hypothesized that autologous bone marrow stem cell transplantation would promote β-cells regeneration by directly differentiated from the transplanted BMMCs or stimulate local stem cells regeneration and thus decrease or eliminate the need of exogenous insulin and improve β-cells function.

Conditions

Interventions

OTHER

BMMCT

Bone marrow mononuclear cell transplantation via selective catheterization

Sponsors & Collaborators

  • Peking University Aerospace Center Hospital

    lead OTHER

Principal Investigators

  • Yizhong Wang, M.D., Ph.D. · Division of Hematology and Endocrinology, Peking University Aerospace Centre Hospital

  • Yuanjie Mao, M.D., Ph.D. · Department of Biochemisty, National Cerebral and Cardiovascular Center; Department of Cardiology, China-Japan Friendship Hospital

  • Lei Lei, M.D. · Division of Hematology and Endocrinology, Peking University Aerospace Centre Hospital

  • Danping Meng, M.D. · Division of Hematology and Endocrinology, Peking University Aerospace Centre Hospital

  • Xiyang Zhang, M.D. · Division of Hematology and Endocrinology, Peking University Aerospace Centre Hospital

  • Xiaolin Jia, M.D. · Division of Hematology and Endocrinology, Peking University Aerospace Centre Hospital

  • Qiuming Jiang, M.D. · Division of Hematology and Endocrinology, Peking University Aerospace Centre Hospital

  • Yufang Li, M.D. · Division of Hematology and Endocrinology, Peking University Aerospace Centre Hospital

  • Song Dong, M.D. · Division of Hematology and Endocrinology, Peking University Aerospace Centre Hospital

  • Liyan Yang, M.D. · Division of Hematology and Endocrinology, Peking University Aerospace Centre Hospital

  • Hong Wang, M.D. · Division of Hematology and Endocrinology, Peking University Aerospace Centre Hospital

  • Mingchao Ding, M.D. · Division of Hematology and Endocrinology, Peking University Aerospace Centre Hospital

  • Liqin Cui, M.D. · Division of Hematology and Endocrinology, Peking University Aerospace Centre Hospital

  • Bin Wang, M.D. · Division of Hematology and Endocrinology, Peking University Aerospace Centre Hospital

  • Xin Lin, M.D. · Division of Hematology and Endocrinology, Peking University Aerospace Centre Hospital

  • Han Shi, M.D. · Division of Hematology and Endocrinology, Peking University Aerospace Centre Hospital

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
30 Years
Max Age
70 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-05-31
Primary Completion
2015-05-31
Completion
2017-07-31

Countries

  • China

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01677013 on ClinicalTrials.gov