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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01249534
Other study ID # EKSG10/144
Secondary ID
Status Completed
Phase N/A
First received November 29, 2010
Last updated December 9, 2010
Start date December 2010
Est. completion date December 2010

Study information

Verified date November 2010
Source Cantonal Hospital of St. Gallen
Contact n/a
Is FDA regulated No
Health authority Switzerland: Ethikkommission
Study type Observational

Clinical Trial Summary

Although widely used, there is a lack of evidence concerning diagnostic value of C-reactive protein (CRP) in the postoperative course. The aim of this study was to evaluate the diagnostic accuracy of CRP for postoperative inflammatory complications after gastroesophageal cancer.


Recruitment information / eligibility

Status Completed
Enrollment 200
Est. completion date December 2010
Est. primary completion date December 2010
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- all patients with gastroesophageal cancer surgery

Exclusion Criteria:

- lack of measurement of C-reactive protein

Study Design

Observational Model: Cohort, Time Perspective: Retrospective


Related Conditions & MeSH terms

  • Given Indication for Gastroesophageal Cancer Surgery

Intervention

Other:
gastroesophageal cancer surgery
gastroesophageal cancer surgery

Locations

Country Name City State
Switzerland Department of surgery St. Gallen

Sponsors (1)

Lead Sponsor Collaborator
Cantonal Hospital of St. Gallen

Country where clinical trial is conducted

Switzerland, 

Outcome

Type Measure Description Time frame Safety issue
Primary postoperative Inflammatory complications 30 days postoperatively No