Full Text View
Tabular View
No Study Results Posted
Related Studies
Acute Phase Proteins as Early Markers in Sepsis
This study is not yet open for participant recruitment.
Verified by University of Zurich, March 2008
First Received: March 17, 2008   Last Updated: March 21, 2008   History of Changes
Sponsored by: University of Zurich
Information provided by: University of Zurich
ClinicalTrials.gov Identifier: NCT00641355
  Purpose

Monitoring of different serumproteins after severe trauma and during trauma-induced sepsis.

  • Trial with surgical intervention

Condition Intervention
Sepsis
Procedure: No intervention

MedlinePlus related topics: Sepsis
U.S. FDA Resources
Study Type: Observational
Study Design: Case-Only, Prospective
Official Title: Acute Phase Proteins as Early Markers in Sepsis

Further study details as provided by University of Zurich:

Biospecimen Retention:   None Retained

Biospecimen Description:

Estimated Enrollment: 15
Study Start Date: April 2008
Estimated Study Completion Date: September 2012
Intervention Details:
    Procedure: No intervention
    No intervention
  Eligibility

Ages Eligible for Study:   18 Years to 65 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population

Patients with severe trauma

Criteria

Inclusion criteria:

  • Patients with severe trauma (ISS score > 16), both genders, patients on ICU

Exclusion criteria:

  • Moribund patients (pH <7,1, lactate >15mmol, Basedeficit > 15mEq/L, severe heart or liver injuries, GCS never over 5 after trauma)
  • Severe head injuries (AIS head >4)
  • Patient with severe infectious diseases, or diseases which severely affect the immune system (diabetes, Alkohol or nicotine abuse)
  • Non-german speaking patients
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00641355

Contacts
Contact: 01 Studienregister MasterAdmins +41 (0)44 255 11 11

Locations
Switzerland
Zurich, Switzerland
Sponsors and Collaborators
University of Zurich
Investigators
Study Director: 01 Studienregister MasterAdmins UniversitaetsSpital Zuerich
  More Information

No publications provided

Responsible Party: University Hospital of Zurich ( PD Dr. Marius Keel )
Study ID Numbers: StV 26-2007
Study First Received: March 17, 2008
Last Updated: March 21, 2008
ClinicalTrials.gov Identifier: NCT00641355     History of Changes
Health Authority: Switzerland: Swissmedic

Study placed in the following topic categories:
Systemic Inflammatory Response Syndrome
Sepsis
Inflammation

Additional relevant MeSH terms:
Systemic Inflammatory Response Syndrome
Sepsis
Pathologic Processes
Infection
Inflammation

ClinicalTrials.gov processed this record on May 06, 2009