Autologous Bone Marrow Mononuclear Cells Therapy in Diabetic Lower Limb Ischemia

Sponsor
Hebei Medical University (Other)
Overall Status
Unknown status
CT.gov ID
NCT01937416
Collaborator
(none)
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Study Details

Study Description

Brief Summary

This study is to evaluate the safety and efficacy of autologous bone marrow mononuclear cells transplantation in diabetic patients with lower limb ischemia.

Condition or Disease Intervention/Treatment Phase
  • Biological: autologous bone marrow mononuclear cells
Phase 1

Detailed Description

Diabetic lower limb ischemia as severe complication of diabetes influences the life quality of patients and currently the effective treatment for the disease is lacking. Bone marrow mononuclear cells have been proved to have multiple functions including the differentiation and proliferation. In animal model, bone marrow mononuclear cells could induce angiogenesis and may have therapeutic usage for ischemia disease. The investigators thereby design the study to investigate the possible therapy of diabetic lower limb ischemia with autologous bone marrow mononuclear cells. Patient with diabetic lower limb ischemia was treated with colony stimulating factor for improvement of bone marrow hematopoiesis. Then bone marrow was taken and mononuclear cells were isolated with deleting erythrocyte by density gradient centrifugation. Bone marrow mononuclear cells were transplanted into ischemia regions of lower limb through intramuscular injection. The investigators investigated the safety of the therapy with life signs like temperature, pulse, blood pressure, routine analysis of blood and urine etc. post the transplantation. And the efficacy was evaluated with the measurement of ulcer size, rest pain score, cold sensation score, resting ABI, resting TcPO2, collateral vessel score and skin microcirculation.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
10 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Safety and Efficacy Investigation of Patients With Diabetic Lower Limb Ischemia by Transplantation of Autologous Bone Marrow Mononuclear Cells
Study Start Date :
Jan 1, 2012
Actual Primary Completion Date :
Sep 1, 2013
Anticipated Study Completion Date :
Dec 1, 2014

Arms and Interventions

Arm Intervention/Treatment
Experimental: autologous bone marrow mononuclear cells

Bone marrow come from the patients himself/herself. With a conventional method and reagent,Ficoll, mononuclear cells were isolated with deleting erythrocyte by density gradient centrifugation.

Biological: autologous bone marrow mononuclear cells
Bone marrow was taken from patient oneself and mononuclear cells were isolated with deleting erythrocyte by density gradient centrifugation. Bone marrow mononuclear cells were transplanted into ischemia regions of lower limb through intramuscular injection.

Outcome Measures

Primary Outcome Measures

  1. Cell transplantation related side effect [2 week after cell transplantation]

    Temperature,pulse,respiration,blood pressure,routine analysis of blood and urine, liver function,renal function,function of coagulation, ECG,cell transplantation related death and cell transplantation related unexpected amputation

Secondary Outcome Measures

  1. ulcer size [Post cell transplantation: 1, 3, 6 months]

    Measuring ulcer area (cm2) and depth (mm)of limb : For each ulcer , photographically record the area and depth with a ruler in order to calculate the ulcer area in square millimeters.

  2. rest pain score [Post cell transplantation: 1,3, 6 months]

    Scoring the rest pain based on the degree of pain as following five scales): 0 level-0 point: no pain; level-1 point: occasional pain which can be recalled; level-2 points: the pain often but can be tolerated, without or with a little analgesics; level-3 points: often with need of general analgesics; level -4 points: affect sleeping due to the pain, general pain medication being difficult to alleviate. Before transplantation: points; after transplantation: points.

  3. cold sensation score [Post cell transplantation: 1,3, 6 months]

    based on a sense of cold as following five scales: 0 level-0 point: no cold sensation; level-1 point, or : Occasionally cold feeling; level-2 points: Often with cold feeling; level-3 points: significantly cold feeling. and can be significantly improved when using a local insulation. level-4 points: significantly cold feeling,and can not be significantly improved when using a local insulation.

  4. Resting ABI [Post cell transplantation: 1,3, 6 months]

    Measurement of ABI(ankle brachial index, ABI): Measure arterial pressure with a laser Doppler, and then calculate the ankle-brachial index, that is a ratio of ankle arterial blood pressure to brachial arterial blood pressure at rest.

  5. Resting TcPO2 (mmHg) [Post cell transplantation:1, 3, 6 months]

    Transcutaneous oxygen pressure(TcPO2) should be measured at the same site in the ischemic limb at rest.

  6. Collateral vessel score [Post cell transplantation: 1,3, 6 months]

    Collateral vessel score: Using computed tomographic angiography to score the collateral vessel formation. A mean score is obtained for each ischemic limb by 3 independent interventionists based on the following 4 level score: 0 (no new collateral vessels) (A little new collateral vessels) (moderate new collateral blood vessels) (Rich new collateral vessels)

  7. Skin microcirculation measurement [1,3,6 months post cell transplantation]

    using PeriMed "laser-Doppler flowmetry" measure the skin microcirculation on the same site in the ischemic limb at rest.

Eligibility Criteria

Criteria

Ages Eligible for Study:
20 Years to 80 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  1. fontaine's stage 2-4 or resting ABI <0.7

  2. age between 20 and 80 years old

  3. sign informed consent, voluntary subjects

  4. diagnosis of diabetic lower limb ischemia

Exclusion Criteria:
  1. poorly controlled diabetes (HBA1c> 7.0%) and proliferative retinopathy (III-IV stage)

  2. malignancy history in the past five years or serum level of tumor markers elevated more than doubled

  3. severe heart, liver, kidney, respiratory failure or poor general condition can not tolerate bone marrow mononuclear cells transplantation

  4. serious infections (such as cellulitis, osteomyelitis, etc.)

  5. pregnant female, or reproductive age female who wants to give birth throughout the course of the study

  6. life expectancy less than half a year

Contacts and Locations

Locations

Site City State Country Postal Code
1 the First Hospital of Hebei Medical University Shijiazhuang Hebei China 050000

Sponsors and Collaborators

  • Hebei Medical University

Investigators

  • Study Chair: Baoyong Yan, Doctor, The First Hospital of Hebei Medical University
  • Study Director: Huimin Zhou, doctor, The First Hospital of Hebei Medical University
  • Principal Investigator: Xu Han, master, The First Hospital of Hebei Medical University
  • Principal Investigator: Quanhai Li, doctor, The First Hospital of Hebei Medical University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Quanhai Li, Director of Cell Thearpy Center, the First Hospital of HeibeiMU, Hebei Medical University
ClinicalTrials.gov Identifier:
NCT01937416
Other Study ID Numbers:
  • 12276102D
First Posted:
Sep 9, 2013
Last Update Posted:
Dec 4, 2013
Last Verified:
Dec 1, 2013
Additional relevant MeSH terms:

Study Results

No Results Posted as of Dec 4, 2013