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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT00548535
Other study ID # DDI1007
Secondary ID
Status Recruiting
Phase N/A
First received October 23, 2007
Last updated October 23, 2007
Start date January 2007
Est. completion date January 2008

Study information

Verified date October 2007
Source University of Zurich
Contact Daniel Dindo, MD
Phone +41 (0)44 255 11 11
Email daniel.dindo@usz.ch
Is FDA regulated No
Health authority Switzerland: Swissmedic
Study type Observational

Clinical Trial Summary

Aim of the study is to evaluate the reliability of self-reported surgical outcome by residents

- prospective assessment of postoperative complications done by residents using a validated five-scale complication classification

- simultanously, complications will be prospectively assessed in the same manner by an external clinical nurse

- Trial with surgical intervention


Recruitment information / eligibility

Status Recruiting
Enrollment 0
Est. completion date January 2008
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 90 Years
Eligibility Inclusion criteria:

- All patients undergoing elective surgery

Exclusion criteria:

- Patients not undergoing surgery

- Patient in outpatient setting

Study Design

Time Perspective: Prospective


Related Conditions & MeSH terms

  • Patients of Visceral- and Transplantation Surgery

Intervention

Procedure:
Reliability of complication assessment


Locations

Country Name City State
Switzerland University Hospital of Zurich Zurich

Sponsors (1)

Lead Sponsor Collaborator
University of Zurich

Country where clinical trial is conducted

Switzerland,