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NCT ID: NCT01876017 Recruiting - Clinical trials for Chronic Renal Failure

Safety and Efficacy of BMMNC in Patients With Chronic Renal Failure

Start date: September 2014
Phase: Phase 1/Phase 2
Study type: Interventional

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

NCT ID: NCT01866072 Recruiting - Clinical trials for Acute on Chronic Liver Failure

Evaluation of Role of Transient Elastography (Fibroscan) in Differentiating Patients of Acute Severe Viral Hepatitis and Acute on Chronic Liver Failure

ACLF
Start date: May 2013
Phase: N/A
Study type: Observational

Transient elastography is novel non-invasive method for assessment of hepatic fibrosis in patients with chronic liver disease, by measuring liver stiffness. Transient elastography is a user friendly technique that can be easily performed at bedside or in outpatient clinic with immediate results and good reproducibility. Liver stiffness values ranges from 2.5 to 75 kPa with lower values <6kPa suggest no fibrosis where as higher values above 14kPa suggests cirrhosis. In the present study the investigators hypothesis that the investigators can differentiate ACLF and acute severe viral hepatitis based on fibroscan as patients with underlying fibrosis with superadded inflammation would have higher fibroscan value than when patient have only inflammation with no underlying fibrosis and hence the investigators can avoid unnecessary test in such subgroup.

NCT ID: NCT01863121 Recruiting - Cirrhosis Clinical Trials

Validation of Child-Turcotte-Pugh-Kumar (CTPK) Score in Predicting Short Term Mortality in Patients With Liver Cirrhosis

Start date: May 2013
Phase: N/A
Study type: Observational

The CTP score is one of the best proved severity score in predicting mortality in patients with cirrhosis. Portal hypertension and variceal bleed are significant causes of morbidity and mortality in patients with cirrhosis. The recently published CTPK score included variceal variceal bleed status to the CTP score which improved the accuracy of CTP score in predicting short term mortality. CTPK score needs prospective validation.

NCT ID: NCT01836562 Recruiting - Autism Clinical Trials

A Clinical Trial to Study the Safety and Efficacy of Bone Marrow Derived Autologous Cells for the Treatment of Autism

BMCA
Start date: September 2014
Phase: Phase 1/Phase 2
Study type: Interventional

This clinical trial is a single Arm, single centre to check the safety and efficacy of bone marrow derived autologous mono nuclear cells (MNC) (100 million per dose). Trial to be conducted for 36 months.

NCT ID: NCT01834664 Recruiting - Clinical trials for Ataxic Infantile Cerebral Palsy

Safety and Efficacy of Bone Marrow Derived Autologous Cells Treatment of Cerebral Palsy in Subjects Above 15 Years

BMACCP
Start date: March 2013
Phase: Phase 1/Phase 2
Study type: Interventional

This Study is Single arm, Single Centre trial to study the safety and efficacy of bone marrow derived autologous mononuclear cells (100 millions per dose)study enrollment duration 36 months sample size 100 patients should be treated (above 15 years of age) with cerebral palsy in India. Primary outcome measures are improvement in walking ability and kinetic gait pattern.

NCT ID: NCT01834079 Recruiting - Optic Atrophy Clinical Trials

Study the Safety and Efficacy of Bone Marrow Derived Autologous Cells for the Treatment of Optic Nerve Disease

OND
Start date: September 2014
Phase: Phase 1/Phase 2
Study type: Interventional

This is a Single arm, Single centre trial to check the safety and efficacy of bone marrow derived autologous mono nuclear cell(100 millions per dose )clinical trial to be conducted for 36 months in patients with optic nerve diseases.

NCT ID: NCT01834066 Recruiting - Muscular Dystrophy Clinical Trials

Study Safety and Efficacy of Bone Marrow Derived Autologous Cells for the Treatment of Muscular Dystrophy.

mdp
Start date: September 2014
Phase: Phase 1/Phase 2
Study type: Interventional

This Study is single arm, single centre trial to check the safety and efficacy of Bone Marrow derived autologous cell(100 million per dose) for the patient with Duchenne Muscular Dystrophy.

NCT ID: NCT01834053 Recruiting - Huntington Disease Clinical Trials

Safety and Efficacy of Bone Marrow Derived MNCs for Treatment of Cells for the Treatment of Hunting Tons Chorea.

BMACHC
Start date: September 2014
Phase: Phase 1/Phase 2
Study type: Interventional

This study is Single arm, Single Centre trial to check the Safety and Efficacy of Bone Marrow Derived Autologous mononuclear cell {MNC} (100 Million per dose).trial to be conducted for 36 months in patients with diabetes Mellitus in India,Primary outcome measure are Improvement in cognitive and Psychiatric Symptoms and Improvement in Jerky,random, and Uncontrollable Movements called Chorea.

NCT ID: NCT01834040 Recruiting - Clinical trials for Duchenne Muscular Dystrophy

Study Safety and Efficacy of BMMNC for the Patient With Duchenne Muscular Dystrophy

BMMNC
Start date: September 2014
Phase: Phase 1/Phase 2
Study type: Interventional

This Study is single arm, single center trial to check the safety and efficacy of BMMNC (100 million per dose) for the patient with Duchenne Muscular Dystrophy,

NCT ID: NCT01833975 Recruiting - Spinal Cord Injury. Clinical Trials

Study the Safety and Efficacy of Bone Marrow Derived Autologous Cells for the Treatment of Spinal Cord Injury

SCI
Start date: September 2014
Phase: Phase 1/Phase 2
Study type: Interventional

This Study is a single arm,Phase I/II , single centre trial to check active comparing the safety and efficacy of Bone marrow derived autologous cell(100 million per dose) trial to be conducted for 36 months.