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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00782704
Other study ID # StV 30-2008
Secondary ID
Status Completed
Phase N/A
First received October 29, 2008
Last updated February 9, 2015
Start date October 2008
Est. completion date December 2009

Study information

Verified date February 2015
Source University of Zurich
Contact n/a
Is FDA regulated No
Health authority Switzerland: Ethic Committee of Kanton Zurich
Study type Observational

Clinical Trial Summary

The aim is to develop and validate a morbidity index for postoperative complications in patients undergoing visceral surgery.


Recruitment information / eligibility

Status Completed
Enrollment 219
Est. completion date December 2009
Est. primary completion date December 2009
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Age: = 18 years

- Capacity to act and no legal guardian

- Patients with any underlying disease admitted to the Department of Visceral and Transplantation Surgery of the University Hospital of Zurich with planned minor or major visceral surgery

- German language as daily language.

Exclusion Criteria:

- Patients with cognitive difficulties and diseases, which may yield unreliable answers

- Patients unable to read and write

Study Design

Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
Switzerland Department of Visceral and Transplantation Surgery of the University Hospital of Zurich 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 to develop and validate a morbidity index preoeprativ and one day before discharge Yes
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