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Difference in Efficacy Between Stem Cell Transplantation and Classical Therapy in Liver Cirrhosis Patients

Difference in Efficacy Between Umbilical Cord Mesenchyma Stem Cell Transplantation and Classical Therapy in Liver Cirrhosis Patients

Status
UNKNOWN
Phases
Phase 1Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01718587
Enrollment
60
Registered
2012-10-31
Start date
2012-11-30
Completion date
2014-07-31
Last updated
2012-10-31

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

Conditions

Liver Cirrhosis

Keywords

umbilical cord mesenchyma stem cell, liver cirrhosis, antiviral therapy

Brief summary

The current treatment methods of liver cirrhosis are limited ,including antiviral therapy,supportive therapy and liver transplantation. Antiviral therapy and Supportive therapy especially the regularly intravenous infusions of plasma or albumin are combined in the clinical classical therapy treatment. In the other hand,umbilical cord mesenchyma stem cell with self and directed differentiation capacity can effectively rescue experimental liver failure and contribute to liver regeneration, which suggests the feasibility of stem cell transplantation therapy. In this study, the safety and efficacy of umbilical cord mesenchyma stem cell transplantation through interventional procedures and classical therapy in patients liver cirrhosis will be evaluated and compared.

Detailed description

This study will includ two research centers, the number of patients in transplantation group will be 30, the number of patients in classical therapy group will be 30. All the inclusion and exclusion criteria will be same and the data analysis will be complete by the epidemiological commissioner.

Interventions

PROCEDUREstem cell transplantation through interventional procedure

interventional procedure once

DRUGantiviral therapy (lamivudine, other antiviral drugs)

lamivudine, 100 mg per day (oral dose); or adefovir dipivoxil 10 mg per day (oral dose); or grace entecavir 0.5-1mg per day (oral dose); or behalftelbivudine 600 mg per day (oral dose).

Sponsors

The First Hospital of Hebei Medical University
CollaboratorOTHER
General Hospital of Chinese Armed Police Forces
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

* Clinical diagnosis of liver cirrhosis; * Without hepatic encephalopathy; * No ascites or have easily dissipated ascites; * Value of bilirubin is less than 100; * Value of albumin is greater than 16 g / L; * Prothrombin time is less than 21 seconds;

Exclusion criteria

* Severe cardiovascular disease, and immunocompromised patients; * Patients with localized lesions affecting graft infection; * Coagulation disorders; * Liver nodules more than 2cm or Liver cancer.

Design outcomes

Primary

MeasureTime frameDescription
change from baseline in liver volume calculated by MRI at 12 months12 months after treatmentInstrument:universal 1.5 Tesla superconducting MRI instrument. Slice thickness :2mm.
change from baseline in liver volume calculated by MRI at 6 months6 months after treatmentInstrument:universal 1.5 Tesla superconducting MRI instrument. Slice thickness :2mm.
liver volume calculated by MRIbaselineInstrument:universal 1.5 Tesla superconducting MRI instrument. Slice thickness :2mm.

Secondary

MeasureTime frameDescription
coagulationbaselin,1,3,6 and 12 months after treatment or transplantation1. prothrombin time (PT) 2. activated partial thromboplastin time (APTT) 3. fibrinogen (FIB) 4. thrombin time (TT)
portal vein and splenic vein measurebaseline,1,3,6 and 12 months after treatment or transplantation1)Portal vein diameter (Dpv) 2)Portal vein maximum velocity (Vmaxpv) 3)Portal vein blood flow per minute (Qpv) 4) The splenic vein diameter (Dsv) 5) Splenic vein maximum flow velocity (Vmaxsv) 6) Splenic vein blood flow per minute (Qsv)
blood biochemistrybaseline, 1,3,6 and 12 months after treatment or transplantation1. alanine aminotransferase 2. aspartate aminotransferase 3. gamma-glutamyltransferase(GGT) 4. alkaline phosphatase 5. total bilirubin 6. direct bilirubin 7. The total bile acid (TBA) 8. albumin 9. the proportion of white balls
estrogen and progestin in bloodbaseline,1,3,6 and 12 months after treatment or transplantationestrogen and progestin
blood testbaseline,1,3,6 and 12 months after treatment or transplantation1. platelet count (PLT) 2. mean platelet volume (MPV) 3. platelet distribution width (PDW) 4. platelet hematocrit (PCT) 5. alpha feto protein (AFP)
liver enzyme fiber spectrumbaseline,1,3,6 and 12 months after treatment or transplantation1. laminin (LN) 2. Ⅳ collagen detection (CIV) 3. hyaluronic acid (HA) 4. procollagen Ⅲ(PC Ⅲ)

Other

MeasureTime frameDescription
gastroscopybaseline,6 and 12 months after treatment or transplantationObserve and photograph the related varicose veins.
liver biopsybaseline,6 and 12 months after transplantationThe result of liver biopsy judged by the same one expert.

Countries

China

Contacts

Primary ContactYihua An, PhD
doctoran2010@hotmail.com0086-10-57976845

Outcome results

None listed

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