NCT01152411

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

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
5

participants targeted

Target at below P25 for phase_1

Timeline
Completed

Started Feb 2010

Typical duration for phase_1

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

February 1, 2010

Completed
5 months until next milestone

First Submitted

Initial submission to the registry

June 26, 2010

Completed
3 days until next milestone

First Posted

Study publicly available on registry

June 29, 2010

Completed
2.3 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

November 1, 2012

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

November 1, 2012

Completed
Last Updated

March 29, 2012

Status Verified

March 1, 2012

Enrollment Period

2.8 years

First QC Date

June 26, 2010

Last Update Submit

March 28, 2012

Conditions

Keywords

Renal FailureChronic Kidney DiseaseChronic Renal Failure

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

EXPERIMENTAL
Other: Autologous bone marrow stem cells

Interventions

Bone marrow stem cells; Single dose; Interventional fluoroscopy-guided injection into the renal artery.

Autologous bone marrow stem cells

Eligibility Criteria

Age18 Years - 65 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

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

Location

MeSH Terms

Conditions

Kidney Failure, ChronicRenal InsufficiencyRenal Insufficiency, Chronic

Condition Hierarchy (Ancestors)

Kidney DiseasesUrologic DiseasesFemale Urogenital DiseasesFemale Urogenital Diseases and Pregnancy ComplicationsUrogenital DiseasesMale Urogenital DiseasesChronic DiseaseDisease AttributesPathologic ProcessesPathological Conditions, Signs and Symptoms

Study Officials

  • Balakrishna S, M.B.B.S

    International Stemcell Services Limited

    STUDY DIRECTOR

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

Locations