Clinical trial · Observational
Application of the Stem Cell Therapy in the End Stage Liver Disease and Assessment Its Consequences in the Quality of Live Style as Well as Development of HCC.
NCT01729221CI-TRIAL-00008514unknownClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
Prospective study to calculated the incidence of hepatocellular carcinoma in hepatitis C virus infected patients after stem cell therapy.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Hepatocellular Carcinoma in Hepatitis C Virus Infected Patients | — | UNRESOLVED | — |
Interventions
Interventions (0)
Data not yet available
No intervention recorded.
Design
Arms and outcomes
Arms (2)
- label
- HCV infected patients treated by stem cell therap
- description
- Hepatitis C virus infected patients treated by stem cell therapy
- label
- HCV infected patients treated by standared line of care
- description
- Hepatitis C virus infected patients treated by standared line of care
Primary outcomes (1)
- measure
- Incidence of hepatocellular carcinoma post stem cell therapy in hepatitis C virus infected patients
- timeFrame
- within the first year after stem cell therapy
Secondary outcomes (1)
- measure
- Compare the incidence of hepatocellular carcinoma in patients who had received stem cell therapy to those who had received the standared line of care
- timeFrame
- within one year of follow up of hepatitis C virus infected patients
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 20 Years
- Maximum age
- 65 Years
Show eligibility criteria text
Inclusion Criteria: * Male or female patients aged from 20 to 65 years of age. * Evidence of chronic liver insufficiency. * The presence of decreased serum albumin and/or increased bilirubin and/or increased international normalized ratio (INR). * Patient is unlikely to receive a liver transplant. * Ability to give written consent * Women of childbearing potential may be included, but must use a reliable and appropriate contraceptive method Exclusion Criteria: * Patients below the age of 20 or above the age of 65 years * Pregnant or lactating women * Patients with recent recurrent GI bleeding or spontaneous bacterial peritonitis * Patients with evidence of HIV or other life threatening infection * Patients unable to give informed consent * Patients with a history of hypersensitivity to G-CSF * Patients who have been included in any other clinical trial within the previous month * Patient with recurrent attacks of hepatic encephalopathy. * Evedince of portal vein thrombosis by ultrasound.
References
Publications (1)
- DERIVEDSalama H, Zekri AR, Medhat E, Al Alim SA, Ahmed OS, Bahnassy AA, Lotfy MM, Ahmed R, Musa S. Peripheral vein infusion of autologous mesenchymal stem cells in Egyptian HCV-positive patients with end-stage liver disease. Stem Cell Res Ther. 2014 May 28;5(3):70. doi: 10.1186/scrt459. PMID 24886681