Novel Preoperative Score Predicting Outcome Following Liver Resection
Sponsor
University of Zurich (Other)
Overall Status
Completed
CT.gov ID
NCT01003197
Collaborator
(none)
1
8
Study Details
Study Description
Brief Summary
To develop and validate a score to predict serious complications following liver resection using pre-operative risk factors.
Condition or Disease | Intervention/Treatment | Phase |
---|---|---|
|
Detailed Description
Liver surgery is associated with a substantial rate of complications. Early identification of patients at risk of serious complications is important in order to adapt therapeutic strategies and to improve quality. The purpose of this study is to develop and validate a score to predict serious complications following liver resection using pre-operative risk factors.
Study Design
Study Type:
Observational
Observational Model:
Cohort
Time Perspective:
Retrospective
Official Title:
Novel Preoperative Score Predicting Outcome Following Liver Resection
Study Start Date
:
Feb 1, 2009
Actual Primary Completion Date
:
Oct 1, 2009
Actual Study Completion Date
:
Oct 1, 2009
Arms and Interventions
Arm | Intervention/Treatment |
---|---|
complication group < III
|
|
complication group >= III
|
Outcome Measures
Primary Outcome Measures
- develop and validate a score to predict serious complications following liver resection using pre-operative risk factors. [postoperative]
Eligibility Criteria
Criteria
Ages Eligible for Study:
18 Years
to 90 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
-
= 18 years
-
liver resection
Exclusion Criteria:
- Trauma cases
Contacts and Locations
Locations
Site | City | State | Country | Postal Code | |
---|---|---|---|---|---|
1 | Department of Visceral and Transplantation Surgery, University Hospital of Zurich | Zürich | Zurich | Switzerland | 8091 |
Sponsors and Collaborators
- University of Zurich
Investigators
- Principal Investigator: Stefan Breitenstein, Dr. med., Department of Visceral and Transplantation Surgery, University Hospital of Zurich
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.Responsible Party:
,
,
ClinicalTrials.gov Identifier:
NCT01003197
Other Study ID Numbers:
- StV 2009
First Posted:
Oct 28, 2009
Last Update Posted:
Oct 28, 2009
Last Verified:
Oct 1, 2009