Skip to content

Safety and Efficacy of BMMNC in Patients With Chronic Renal Failure

An Open Labeled Clinical Study to Evaluate the Safety and Efficacy of of Bone Marrow Derived Mono Nuclear Stem Cell (BMMNCs) in Chronic Renal Failure Patients. It is Self Funded (Patients' Own Funding) Clinical Trial

Status
UNKNOWN
Phases
Phase 1Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01876017
Enrollment
15
Registered
2013-06-12
Start date
2014-09-30
Completion date
2016-12-31
Last updated
2014-09-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic Renal Failure

Keywords

CRF, STEM CELL, CKD

Brief summary

This Study is single arm, single center trial to check the safety and efficacy of Autologous Bone Marrow derived Mono Nuclear Stem Cell (BMMNCs)for the patient with CRF

Detailed description

Chronic kidney failure, also called chronic kidney disease, describes the gradual loss of kidney function. Kidney failure is a medical condition in which kidneys fail to filter metabolic wastes and toxins out of the body and a series of symptoms will be developed .It is common, frequently un recognised and often exists together with other conditions (for example, cardiovascular disease and diabetes). When advanced, it also carries a higher risk of mortality. The risk of developing CKD(Chronic Kidney diseases ) increases with increasing age, and some conditions that coexist with CKD become more severe as kidney dysfunction advances CKD can progress to established renal failure in a small but significant percentage of people. This classification divides CKD into five stages. Stages 3-5 may be defined by glomerular filtration rate (GFR) alone, whereas stages 1 and 2 also require the presence of persistent proteinuria, albuminuria or haematuria, or structural abnormalities. Stem cells have two important characteristics that distinguish them from other types of cells. First, they are unspecialized cells that renew themselves for long periods through cell division. The second is that under certain physiologic or experimental conditions, they can be induced to become cells with special function such as the beating cells of heart muscle or the insulin- producing cells of the pancreas as well as the neurons of brain.So our approach is to prove safety and efficacy of stem cell in CRF

Interventions

BIOLOGICALIntravenous transfer of Autologous (BMMNCs)

Intervention therapy , Total 3 doses ,in 30 days ,in 7days interval Intravenous transfer of Autologous (BMMNCs)

Sponsors

Chaitanya Hospital, Pune
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

* Age limit: 18 -65 * willingness to undergo Bone marrow and umbilical cord derived Mesenchymal stem cell transplantation. * To give an informed consent as well as sign the required Informed Consent Form (ICF) for the study. * willingness to regularly visit the hospital / clinic for follow up during the follow up period / on prior agreed time points as per the protocol.

Exclusion criteria

* Patients with pre-existing or current systemic disease such as lung , liver (exception: history of uncomplicated hepatitis A) gastrointestinal , cardiac, immunodeficiency (including HIV) or any other condition determined by history or laboratory investigation that could cause a neurological defect (including syphilis, clinically relevant polyneuropathy) etc. * Women who are pregnant or lactating * Chronic kidney disease due to autoimmune aetiology, connective tissue disease, amyloidosis and storage disorders. * Suffering from Severe co-morbidities like cardiac insufficiency, congestive cardiac failure, malignancy, infection, sepsis and bed sores. * Positive test results for HIV and AIDS complex ,HCV (hepatitis C virus ), HbsAg and Syphilis * Hemoglobin level below 7g % * estimated glomerular filtration rate (eGFR) of \< 45ml/min

Design outcomes

Primary

MeasureTime frameDescription
Maintain or demonstrate improvement in laboratory values.3 month• Hematological (Complete blood count (CBC) Complete blood count (CBC) urea(mg/dL), creatinine (mg/dL), plasma calcium(mg/dL), plasma alkaline phosphatase (U/L),plasma phosphorus (mg/dL), plasma cholesterol(mg/dL), plasma HDL-cholesterol (mg/dL), plasma triglyceride (mg/dL), hematocrit (%) and erythrocyte(M/\_L) values were evaluated before and at the end of the study.)

Secondary

MeasureTime frameDescription
pain intensity by VAS3 monthAssessment of pain by visual analogue score
Improvement in SF36(Short form 36) score3 monthThe SF36, a short-form QoL scoring system with 36 items, is a self-administered questionnaire that was constructed to fill the gap between much more lengthy surveys and relatively coarse single-item measures of the QoL
Improvement in subjective global assessment3 month
the incident of uremia and dialysis requirement6 month

Countries

India

Contacts

Primary ContactSachin P Jamadar, D.Ortho
sac2751982@gmail.com918888788880

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026