Clinical Trials Logo

Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT00564109
Other study ID # StV 10-2003
Secondary ID
Status Recruiting
Phase N/A
First received November 26, 2007
Last updated March 17, 2008
Start date August 2005
Est. completion date January 2008

Study information

Verified date November 2007
Source University of Zurich
Contact 01 Studienregister MasterAdmins
Phone +41 (0)44 255 11 11
Is FDA regulated No
Health authority Switzerland: Swissmedic
Study type Observational

Clinical Trial Summary

Retrospective analysis of PSP- and PAP-serum levels in trauma patients with soft tissue defects and possible correlation with the incidence and onset of infection and sepsis.


Recruitment information / eligibility

Status Recruiting
Enrollment 15
Est. completion date January 2008
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 65 Years
Eligibility Inclusion criteria:

- Trauma patients submitted to the university hospital Zurich, aged 18-65 with soft tissue defects

Exclusion criteria:

- Patients with known immunocompromising illnesses, drug abuse or infectious diseases.

Study Design

Observational Model: Cohort, Time Perspective: Retrospective


Related Conditions & MeSH terms

  • Trauma Patients With Soft Tissue Defects

Intervention

Procedure:
retrospective Observation
retrospective Observation

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
University of Zurich

Country where clinical trial is conducted

Switzerland,