Safety and Efficacy of Autologous Bone Marrow Stem Cells for Treating Chronic Renal Failure
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)
1 other identifier
interventional
5
1 country
1
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for phase_1
Started Feb 2010
Typical duration for phase_1
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
February 1, 2010
CompletedFirst Submitted
Initial submission to the registry
June 26, 2010
CompletedFirst Posted
Study publicly available on registry
June 29, 2010
CompletedPrimary Completion
Last participant's last visit for primary outcome
November 1, 2012
CompletedStudy Completion
Last participant's last visit for all outcomes
November 1, 2012
CompletedMarch 29, 2012
March 1, 2012
2.8 years
June 26, 2010
March 28, 2012
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
Significant clinical improvement in serum creatinine and urine output (improvement in measured GFR by 50%)
1 year
Number of patients reporting adverse effects as a measure of safety and tolerability
1 year
Secondary Outcomes (1)
Improvement in renal biopsy
1 year
Study Arms (1)
Autologous bone marrow stem cells
EXPERIMENTALInterventions
Bone marrow stem cells; Single dose; Interventional fluoroscopy-guided injection into the renal artery.
Eligibility Criteria
You may qualify if:
- 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.
You may not qualify if:
- 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
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
St. Theresa's Hospital
Bengaluru, Karnataka, 560010, India
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- STUDY DIRECTOR
Balakrishna S, M.B.B.S
International Stemcell Services Limited
Study Design
- Study Type
- interventional
- Phase
- phase 1
- Allocation
- NA
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- INDUSTRY
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
June 26, 2010
First Posted
June 29, 2010
Study Start
February 1, 2010
Primary Completion
November 1, 2012
Study Completion
November 1, 2012
Last Updated
March 29, 2012
Record last verified: 2012-03