Status:

UNKNOWN

A Clinical Study to Evaluate the Safety and Efficacy of Mesenchymal Stem Cells in Liver Cirrhosis

Lead Sponsor:

Chaitanya Hospital, Pune

Conditions:

Liver Cirrhosis

Eligibility:

All Genders

25-65 years

Phase:

PHASE1

PHASE2

Brief Summary

Cirrhosis is caused by sustained liver damage over several years either by alcohol, viral infection (Hepatitis B, C), a toxic substance (for eg. drugs, excess copper or iron in the liver), or by block...

Detailed Description

In this study, the patients with liver cirrhosis will undergo administration of human Mesenchymal stem cell MSCs intravenously for these patients.To observe the results Liver function will be monitore...

Eligibility Criteria

Inclusion

  • Inclusion Criteria
  • 25 -65 Ages Eligible for Study
  • Clinical diagnosis of liver cirrhosis
  • Ability to comprehend the explained protocol and thereafter give an informed consent as well as sign the required Informed Consent Form (ICF) for the study.
  • Expecting lifetime is over three years
  • Ready to come all visits
  • Exclusion Criteria:
  • History of life threatening allergic or immune-mediated reaction
  • Positive test results for HIV and AIDS complex ,HCV , HbsAg and Syphilis
  • Malignancies
  • Sepsis
  • Vital organs failure
  • Pregnant or lactating women
  • Subject who has been transplanted recently
  • If the investigator or treating physician feels that the Subject with any disease or condition would interfere with the trial or the safety of patient

Exclusion

    Key Trial Info

    Start Date :

    December 1 2013

    Trial Type :

    INTERVENTIONAL

    Allocation :

    ESTIMATED

    End Date :

    December 1 2014

    Estimated Enrollment :

    20 Patients enrolled

    Trial Details

    Trial ID

    NCT01877759

    Start Date

    December 1 2013

    End Date

    December 1 2014

    Last Update

    October 9 2013

    Active Locations (1)

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    Page 1 of 1 (1 locations)

    1

    Chaitanya Hospital

    Pune, Maharashtra, India, 411009