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Evaluation for the effectiveness and safety for Autologous Bone Marrow Cell infusion (ABMi) therapy for HCV infected liver cirrhosis patient.

Not Applicable
Recruiting
Conditions
HCV infection, Liver cirrhosis
Registration Number
JPRN-UMIN000011651
Lead Sponsor
Yamaguchi University Graduate School of Medicine
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
34
Inclusion Criteria

Not provided

Exclusion Criteria

(1) Liver cirrhosis induced by other factor without HCV infection and unknown reasons (2) have a malignant neoplasm, or a history of malignant neoplasm (Including HCC) (3) have risk of Esophageal or/and gastric varices (4) Renal dysfunction with 2mg/dL or higher serum creatinine (5) hemoglobin under 8g/dL or Platelets under 50/mL or Prothrombin activity under 40% (6) Total bilirubin 3.0mg/dL or more (7) Performance Status 3 or 4 (8) Cases that cannot obtain the informed consent to autologous blood transfusion (9) undeniable possibility for HBV infection, HIV infection, ATL infection, human parvovirus B19 infection (10) Pregnancy (11) not fit for general anesthesia (12) have a severe allergic reaction to contrast dye or a history of a severe allergic reaction to contrast dye (13) other conditions that doctor considered not suitable for the study

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Improvement of Child-Pugh score at 24 weeks after ABMi therapy and control
Secondary Outcome Measures
NameTimeMethod
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