Novel Preoperative Score Predicting Outcome Following Liver Resection
This study has been completed.
Sponsor:
University of Zurich
Information provided by:
University of Zurich
ClinicalTrials.gov Identifier:
NCT01003197
First received: October 27, 2009
Last updated: NA
Last verified: October 2009
History: No changes posted
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Purpose
To develop and validate a score to predict serious complications following liver resection using pre-operative risk factors.
| Condition |
|---|
|
Serious Complications Following Liver Resection |
| Study Type: | Observational |
| Study Design: | Observational Model: Cohort Time Perspective: Retrospective |
| Official Title: | Novel Preoperative Score Predicting Outcome Following Liver Resection |
Further study details as provided by University of Zurich:
Primary Outcome Measures:
- develop and validate a score to predict serious complications following liver resection using pre-operative risk factors. [ Time Frame: postoperative ] [ Designated as safety issue: Yes ]
| Study Start Date: | February 2009 |
| Study Completion Date: | October 2009 |
| Primary Completion Date: | October 2009 (Final data collection date for primary outcome measure) |
| Groups/Cohorts |
|---|
| complication group < III |
| complication group >= III |
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.
Eligibility| Ages Eligible for Study: | 18 Years to 90 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
| Sampling Method: | Probability Sample |
Study Population
HPB center Zurich, Switzerland
Criteria
Inclusion Criteria:
- >= 18 years
- liver resection
Exclusion Criteria:
- Trauma cases
Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT01003197
Locations
| Switzerland | |
| 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 |
More Information
No publications provided
| Responsible Party: | Breitenstein Stefan, Dr. med., Department of Visceral- and Transplantation Surgery |
| ClinicalTrials.gov Identifier: | NCT01003197 History of Changes |
| Other Study ID Numbers: | StV 2009 |
| Study First Received: | October 27, 2009 |
| Last Updated: | October 27, 2009 |
| Health Authority: | Switzerland: Ethikkommission |
Keywords provided by University of Zurich:
|
Development Validation Prediction Score |
Complication Liver resection develop and validate a score to predict serious complications following liver resection using pre-operative risk factors. |
ClinicalTrials.gov processed this record on May 19, 2013