Novel Prediction Score for Postoperative Acute Renal Failure (ARF) Following Liver Resection
NCT ID: NCT00743132
Last Updated: 2010-01-25
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
569 participants
OBSERVATIONAL
2008-04-30
2008-12-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
There is limited evidence on the incidence of postoperative ARF and its clinical relevance in patients undergoing liver resection.
This study will evaluate the incidence of acute renal failure (ARF) after liver resection and its impact on postoperative mortality.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Predicting Acute-on-Chronic Liver Failure After Surgical Intervention in Chronic Liver Disease
NCT04578301
Novel Preoperative Score Predicting Outcome Following Liver Resection
NCT01003197
Characterization and Pathogenesis of ACLF
NCT04975490
Preoperative Evaluation of the Remaining Part of the Liver for Liver Resection
NCT04100304
ARAPS Study on Accelerated Liver Regeneration
NCT04107324
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
There is limited evidence on the incidence of postoperative ARF and its clinical relevance in patients undergoing liver resection.
This study will evaluate the incidence of acute renal failure (ARF) after liver resection and its impact on postoperative mortality.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
COHORT
RETROSPECTIVE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
1
Postoperative no renal dysfunction
No interventions assigned to this group
2
Postoperative renal dysfunction
No interventions assigned to this group
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Benign and malign liver diseases
Exclusion Criteria
18 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
University of Zurich
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Swiss HPB (Hepato-Pancreato-Biliary) Center, Department of Surgery
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Swiss HPB (Hepato-Pancreato-Biliary) Center of the University Hospital Zurich
Zurich, Canton of Zurich, Switzerland
Countries
Review the countries where the study has at least one active or historical site.
References
Explore related publications, articles, or registry entries linked to this study.
Slankamenac K, Breitenstein S, Held U, Beck-Schimmer B, Puhan MA, Clavien PA. Development and validation of a prediction score for postoperative acute renal failure following liver resection. Ann Surg. 2009 Nov;250(5):720-8. doi: 10.1097/SLA.0b013e3181bdd840.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
StV 11-2008
Identifier Type: -
Identifier Source: secondary_id
StV 11-2008
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.