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Clinical Trials/NCT00930085
NCT00930085CompletedNot Applicable

Evaluation of Predictive Proteic Profile on Mortality in the Acute Phase of Septic Shock in Cancer Patients

Institut Paoli-Calmettes1 site in 1 country60 target enrollmentStarted: August 1, 2008Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
60
Locations
1
Primary Endpoint
Identification and characterization of early proteic biomarkers predictive of short term mortality in cancer patients with septic shock.

Study Overview

Brief Summary

The mortality induced by infections in onco-hematological patients is abnormally high at the acute phase of septic shock. Consequently, it is important to detect the population with a high risk of short term mortality among patients with a septic shock. The aim of this study is the evaluation of predictive proteic profile on the short term mortality in the acute phase of septic shock in cancer patients.

Detailed Description

Method: Monocentric prospective study with diagnostic and prognostic expectations.

Primary objective:

Identification and characterization of early proteic biomarkers predictive of short term mortality in cancer patients with septic shock.

Secondary objective:

Research of clinical and biological prognostic factors.

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Patient from oncology or hematology with a septic shock
  • Patient aged 18 years and older
  • Inclusion within the 24 hours of the septic shock in the intensive care unit
  • Signed consent according to the emergency reglementation

Exclusion Criteria

  • Pregnancy, breast feeding
  • Patient with decision of care limitation
  • Patient with legal protection

Outcomes

Primary Outcomes

Identification and characterization of early proteic biomarkers predictive of short term mortality in cancer patients with septic shock.

Time Frame: 1 month

Secondary Outcomes

  • Research of clinical and biological prognostic factors.(1 month)

Investigators

Sponsor
Institut Paoli-Calmettes
Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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