Now Available for Public Comment: Notice of Proposed Rulemaking (NPRM) for FDAAA 801 and NIH Draft Reporting Policy for NIH-Funded Trials

Prospective Evaluation of Predictors for Organ Failure Following Liver Transplantation

This study has been completed.
Sponsor:
Information provided by:
Heidelberg University
ClinicalTrials.gov Identifier:
NCT00408889
First received: December 6, 2006
Last updated: April 8, 2010
Last verified: December 2008

December 6, 2006
April 8, 2010
December 2006
Not Provided
Not Provided
Not Provided
Complete list of historical versions of study NCT00408889 on ClinicalTrials.gov Archive Site
Not Provided
Not Provided
Not Provided
Not Provided
 
Prospective Evaluation of Predictors for Organ Failure Following Liver Transplantation
Prospective Evaluation of Predictors for Organ Failure Following Liver Transplantation

Early organ failure occurs frequently and is difficult to predict. The study aims to define a predictive score for early transplant failure.

Patients will be monitored 7 days following liver transplantation, including clinical scores, clinical chemistry, ultrasound findings and indocyaninegreen-clearance.

Observational
Observational Model: Cohort
Time Perspective: Prospective
Not Provided
Not Provided
Non-Probability Sample

Patients undergoing liver transplantation

Liver Transplantation
Not Provided
Not Provided
Schneider L, Spiegel M, Latanowicz S, Weigand MA, Schmidt J, Werner J, Stremmel W, Eisenbach C. Noninvasive indocyanine green plasma disappearance rate predicts early complications, graft failure or death after liver transplantation. Hepatobiliary Pancreat Dis Int. 2011 Aug;10(4):362-8.

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
150
Not Provided
Not Provided

Inclusion Criteria:

  • orthotopic liver transplantation
  • age > 18 years

Exclusion Criteria:

  • allergy to indocyangreen
Both
18 Years to 80 Years
No
Contact information is only displayed when the study is recruiting subjects
Germany
 
NCT00408889
post OLT
Not Provided
Not Provided
Heidelberg University
Not Provided
Principal Investigator: Christoph Eisenbach, Dr. Heidelberg University
Heidelberg University
December 2008

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP