NCT01412593

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

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
50

participants targeted

Target at P50-P75 for phase_1

Timeline
Completed

Started Sep 2011

Typical duration for phase_1

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

August 8, 2011

Completed
1 day until next milestone

First Posted

Study publicly available on registry

August 9, 2011

Completed
23 days until next milestone

Study Start

First participant enrolled

September 1, 2011

Completed
1 year until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 1, 2012

Completed
1 year until next milestone

Study Completion

Last participant's last visit for all outcomes

September 1, 2013

Completed
Last Updated

August 9, 2011

Status Verified

May 1, 2011

Enrollment Period

1 year

First QC Date

August 8, 2011

Last Update Submit

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

EXPERIMENTAL
Biological: Stem cell transplant

Control

NO INTERVENTION

Interventions

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.

Stem cell transplant

Eligibility Criteria

Age18 Years - 75 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

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

Location

MeSH Terms

Conditions

End Stage Liver Disease

Interventions

Stem Cell Transplantation

Condition Hierarchy (Ancestors)

Liver FailureHepatic InsufficiencyLiver DiseasesDigestive System Diseases

Intervention Hierarchy (Ancestors)

Cell TransplantationCell- and Tissue-Based TherapyBiological TherapyTherapeuticsTransplantationSurgical Procedures, Operative

Central Study Contacts

Ayman Abdo, Associate Professor

CONTACT

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

Locations