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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01003197
Other study ID # StV 2009
Secondary ID
Status Completed
Phase N/A
First received October 27, 2009
Last updated October 27, 2009
Start date February 2009
Est. completion date October 2009

Study information

Verified date October 2009
Source University of Zurich
Contact n/a
Is FDA regulated No
Health authority Switzerland: Ethikkommission
Study type Observational

Clinical Trial Summary

To develop and validate a score to predict serious complications following liver resection using pre-operative risk factors.


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.


Recruitment information / eligibility

Status Completed
Enrollment 0
Est. completion date October 2009
Est. primary completion date October 2009
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 90 Years
Eligibility Inclusion Criteria:

- >= 18 years

- liver resection

Exclusion Criteria:

- Trauma cases

Study Design

Observational Model: Cohort, Time Perspective: Retrospective


Related Conditions & MeSH terms

  • Serious Complications Following Liver Resection

Locations

Country Name City State
Switzerland Department of Visceral and Transplantation Surgery, University Hospital of Zurich Zürich Zurich

Sponsors (1)

Lead Sponsor Collaborator
University of Zurich

Country where clinical trial is conducted

Switzerland, 

Outcome

Type Measure Description Time frame Safety issue
Primary develop and validate a score to predict serious complications following liver resection using pre-operative risk factors. postoperative Yes