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Safety and Efficacy of Autologous Bone Marrow Stem Cells for Treating Chronic Renal Failure

Primary Purpose

Chronic Renal Failure

Status
Unknown status
Phase
Phase 1
Locations
India
Study Type
Interventional
Intervention
Autologous bone marrow stem cells
Sponsored by
International Stemcell Services Limited
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Chronic Renal Failure focused on measuring Renal Failure, Chronic Kidney Disease, Chronic Renal Failure

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Must be able to give voluntary written (patients may not be able to write) consent.
  2. Must be able to understand study information provided to him.
  3. CKD patients of stage IV and ESRD with age 18 to 65 years.
  4. Patient should be afebrile 24 hours prior to procedure.

Exclusion Criteria:

  • Women who are pregnant or lactating
  • Acute Renal Failure
  • Severe co-morbidities like cardiac insufficiency, congestive cardiac failure, malignancy, infection, sepsis and bed sores.
  • Haemoglobin level below 8g %
  • Chronic kidney disease due to autoimmune aetiology, connective tissue disease, amyloidosis and storage disorders.
  • Known bleeding or coagulation disorder.
  • Known hematologic disease
  • Poorly controlled hypertension
  • Evidence of active malignancy within one year prior to randomization.
  • Severe skin infection or osteomyelitis - the site of bone marrow aspiration potentially limiting the procedure.
  • Have a known allergy to iodinated contrast
  • Positive test results for HIV and AIDS complex, HCV, HbsAg and Syphilis.
  • History of drug or alcohol abuse
  • Patients on immunosuppressive therapy

Sites / Locations

  • St. Theresa's Hospital

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Autologous bone marrow stem cells

Arm Description

Outcomes

Primary Outcome Measures

Significant clinical improvement in serum creatinine and urine output (improvement in measured GFR by 50%)
Number of patients reporting adverse effects as a measure of safety and tolerability

Secondary Outcome Measures

Improvement in renal biopsy

Full Information

First Posted
June 26, 2010
Last Updated
March 28, 2012
Sponsor
International Stemcell Services Limited
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1. Study Identification

Unique Protocol Identification Number
NCT01152411
Brief Title
Safety and Efficacy of Autologous Bone Marrow Stem Cells for Treating Chronic Renal Failure
Official Title
Use of Autologous Bone Marrow Stem Cell Transplantation in the Treatment of Chronic Renal Failure in 5 Indian Patients - ABMST-CRF Study (Autologous Bone Marrow Stem Cell Transplantation-CRF)
Study Type
Interventional

2. Study Status

Record Verification Date
March 2012
Overall Recruitment Status
Unknown status
Study Start Date
February 2010 (undefined)
Primary Completion Date
November 2012 (Anticipated)
Study Completion Date
November 2012 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
International Stemcell Services Limited

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Chronic renal failure (CRF, or "chronic kidney failure", CKF, or "chronic kidney disease", CKD) is a slowly progressive loss of renal function over a period of months or years and defined as an abnormally low glomerular filtration rate, which is usually determined indirectly by the creatinine level in blood serum. CRF that leads to severe illness and requires some form of renal replacement therapy(such as dialysis) is called end-stage renal disease (ESRD). While renal replacement therapies can maintain patients indefinitely and prolong life, the quality of life is severely affected. Renal transplantation increases the survival of patients with stage 5 CKD significantly when compared to other therapeutic options; however, it is associated with an increased short-term mortality (due to complications of the surgery). In view of the above, there is definitely an urgent need for finding different methods of treatment for these patients who cannot undergo established modalities of treatment or these have been tried unsuccessfully hence the inadequacy of current treatment modalities and insufficiency of donor organs for transplantation have driven a search for improved methods of dealing with renal failure. The rising concept of cell-based therapeutics has provided a framework around which new approaches are being generated, and its combination with advances in stem cell research stands to bring both fields to clinical fruition. Since CRF affects a large number of these patients who will lose their productive life, stem cell implantation can offer some promise of improved health. In our present study, we want to evaluate the safety and efficacy (to know / observe for Proof of concept in five indian patients) if any, of autologous bone marrow derived stem cells injected into the Renal Artery in five (initially five patients, can be increased to ten patients after observing the initial results) patients with Chronic Renal Failure.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Renal Failure
Keywords
Renal Failure, Chronic Kidney Disease, Chronic Renal Failure

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1, Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
5 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Autologous bone marrow stem cells
Arm Type
Experimental
Intervention Type
Other
Intervention Name(s)
Autologous bone marrow stem cells
Intervention Description
Bone marrow stem cells; Single dose; Interventional fluoroscopy-guided injection into the renal artery.
Primary Outcome Measure Information:
Title
Significant clinical improvement in serum creatinine and urine output (improvement in measured GFR by 50%)
Time Frame
1 year
Title
Number of patients reporting adverse effects as a measure of safety and tolerability
Time Frame
1 year
Secondary Outcome Measure Information:
Title
Improvement in renal biopsy
Time Frame
1 year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Must be able to give voluntary written (patients may not be able to write) consent. Must be able to understand study information provided to him. CKD patients of stage IV and ESRD with age 18 to 65 years. Patient should be afebrile 24 hours prior to procedure. Exclusion Criteria: Women who are pregnant or lactating Acute Renal Failure Severe co-morbidities like cardiac insufficiency, congestive cardiac failure, malignancy, infection, sepsis and bed sores. Haemoglobin level below 8g % Chronic kidney disease due to autoimmune aetiology, connective tissue disease, amyloidosis and storage disorders. Known bleeding or coagulation disorder. Known hematologic disease Poorly controlled hypertension Evidence of active malignancy within one year prior to randomization. Severe skin infection or osteomyelitis - the site of bone marrow aspiration potentially limiting the procedure. Have a known allergy to iodinated contrast Positive test results for HIV and AIDS complex, HCV, HbsAg and Syphilis. History of drug or alcohol abuse Patients on immunosuppressive therapy
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Balakrishna S, M.B.B.S
Organizational Affiliation
International Stemcell Services Limited
Official's Role
Study Director
Facility Information:
Facility Name
St. Theresa's Hospital
City
Bengaluru
State/Province
Karnataka
ZIP/Postal Code
560010
Country
India

12. IPD Sharing Statement

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Safety and Efficacy of Autologous Bone Marrow Stem Cells for Treating Chronic Renal Failure

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