Intra-hepatic Artery Bone Marrow Derived Stem Cells Infusion for the Treatment of Advanced Liver Cirrhosis
1 other identifier
interventional
50
1 country
1
Brief Summary
Liver disease is a common medical problem in Saudi Arabia. Early studies indicated that around 10% of the Saudi population is either infected with hepatitis B or C. An estimated 12% of chronic HCV and HBV patients undergoing liver biopsy from Saudi centers have cirrhosis. Of these 3-5% would decompensate yearly thereby requiring liver transplantation. Based on the most recent national census figures, and a 1-2% prevalence rate of HBV and HCV nationwide, an estimated 1,000 patients would require liver transplantation on a yearly basis for decompensated cirrhosis. Liver transplantation is the only available life saving treatment for patients with end stage liver disease. Unfortunately less than 100 liver transplantations are performed in Saudi Arabia in three centers. Around 100 other patients travel abroad for transplantation annually while all other patients progressively deteriorate and eventually die from the complications of decompensated liver cirrhosis. In addition, even in patients who are listed for liver transplantation, often patients are too sick to wait on the transplant list that often takes more than a year and the on-list mortality is high. A procedure or an intervention that may help to stabilize liver function in order to help patients survive on the transplant list while awaiting liver transplantation would be of immense benefit. Examples of such interventions are already approved and used in some centers like the MARS system.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for phase_1
Started Sep 2011
Typical duration for phase_1
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
August 8, 2011
CompletedFirst Posted
Study publicly available on registry
August 9, 2011
CompletedStudy Start
First participant enrolled
September 1, 2011
CompletedPrimary Completion
Last participant's last visit for primary outcome
September 1, 2012
CompletedStudy Completion
Last participant's last visit for all outcomes
September 1, 2013
CompletedAugust 9, 2011
May 1, 2011
1 year
August 8, 2011
August 8, 2011
Conditions
Outcome Measures
Primary Outcomes (1)
Improvement of liver function measured by improvement in the model for end-stage liver disease (MELD) score.
2 years
Study Arms (2)
Stem cell transplant
EXPERIMENTALControl
NO INTERVENTIONInterventions
Patients randomized to the intervention arm will be admitted to the Liver Care Unit. Granulocyte colony-stimulating factor (G-CSF; 300mcg/mL) will be administered for 1 day as a single daily subcutaneous dose. This dose is sufficient to induce 10 folds enrichment for bone marrow cells.
Eligibility Criteria
You may qualify if:
- Age \>18 years
- Clinically diagnosed liver cirrhosis by any of the following: ultrasound/MRI/ CT/ + tissue biopsy.
- MELD score ≥ 18 and \<35
- Ability to sign an informed consent
- Refused by liver transplant program or labeled as not a liver transplant candidate, decided by at least 3 transplant physicians
You may not qualify if:
- On a liver transplantation waiting list
- Questionable diagnosis of cirrhosis
- Prior history of organ transplantation
- Probable or diagnosis of hepatocellular carcinoma
- Major hepatic vascular thrombosis (hepatic artery, or portal or hepatic veins)
- Serious cardiovascular or respiratory disease, or other medical condition with a high anticipated mortality within twelve months
- Current or recent (within the past 4 weeks) use of vasoactive drugs (Epinephrine, Norepinephrine, Vasopressin, Dopamine, terlipressin)
- Type-1 (acute) hepatorenal syndrome
- Levels of serum creatinine \>150 µmol/ml and/or creatinine clearance \<30 ml/min (as calculated by MDRD system)
- Documented or suspected ongoing infection
- Active or recent gastrointestinal bleeding episode (in the previous 4 weeks)
- Active alcohol abuse extending to within the previous six months
- Pulmonary hypertension (PAP \> 35 mmHg), porto-pulmonary hypertension or hepatopulmonary syndrome
- Pregnancy
- HIV infection
- +5 more criteria
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
King Khalid University Hospital
Riyadh, Riyadh Region, 11461, Saudi Arabia
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- phase 1
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
Study Record Dates
First Submitted
August 8, 2011
First Posted
August 9, 2011
Study Start
September 1, 2011
Primary Completion
September 1, 2012
Study Completion
September 1, 2013
Last Updated
August 9, 2011
Record last verified: 2011-05