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Liver Regeneration Therapy Using Autologous Adipose Tissue Derived Stromal Cells

Liver Regeneration Therapy Using Autologous Adipose Tissue Derived Stromal Cells

Status
Terminated
Phases
Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00913289
Enrollment
6
Registered
2009-06-04
Start date
2009-02-28
Completion date
2010-04-30
Last updated
2012-10-18

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

Conditions

Liver Cirrhosis

Keywords

Liver Cirrhosis

Brief summary

Mesenchymal stem cells have the capability to differentiate into hepatocytes and will be useful for liver regeneration. Adipose tissue is relatively enriched with mesenchymal stem cells compared to bone marrow tissue. In this trial, eligible liver cirrhosis patients will receive autologous adipose tissue derived stromal cells which include such mesenchymal stem cells.

Detailed description

The population of the liver cirrhosis patients is enormous in Japan and the only radical treatment for them is liver transplantation. However, the number of giving donors is extremely limited. Mesenchymal stem cells have been capable to differentiate into mesodermal-lineage cells as well as endodermal-lineage cells such as hepatocytes. They reside in the mesenchymal tissues such as bone marrows as well as adipose tissues. The latter tissues are relatively enriched with mesenchymal stem cells compared to bone marrow cells. In this study, the cirrhotic patients will receive autologous adipose tissue derived stromal cells which contains substantial number of mesenchymal stem cells.

Interventions

BIOLOGICALadipose tissue derived stromal cells

dosage

Sponsors

Kanazawa University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
20 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* Liver cirrhosis patients * Platelets count in peripheral blood: over 7.0x10\^4/microliter * Serum creatinine: less than 1.5 mg/dl * Capable of understanding the features of this clinical trial

Exclusion criteria

* Associated with risky gastroesophageal varices for bleeding * Severe portal hypertension * Complicated with severe heart failure * Renal disease * Respiratory disease * Hematological disease * Coagulation disturbance and judged to be excluded by doctors * Associated with malignancy * Past history of the following: * malignancy * ischemic heart disease * cerebrovascular disease (cerebral infarction, cerebral hemorrhage) * decompensated status of liver cirrhosis * Pregnant, or possibility of pregnancy * Infected with HIV * Under mediation with adrenal corticoid steroid, anti-histamine drug * Anticipated with difficulty of follow-up observation * Anticipated with inconsistency of following the protocol * Addiction of alcohol drinking and unable to stop drinking * Other candidates who are judged to be not applicable to this study by doctors

Design outcomes

Primary

MeasureTime frame
all cause harmful events6 months

Countries

Japan

Outcome results

None listed

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