Study of the Proteome and Cytokines During Inflammatory Syndromes of Different Etiologies.
Proteome
1 other identifier
interventional
97
1 country
1
Brief Summary
The hypotheses of our research are based on the fact that various pathological states, infection, cancer, inflammatory disease, can induce an inflammatory syndrome, through different pathways, even though the clinical presentation can be identical. The identification of biological markers specific to an etiology would therefore allow a faster diagnosis and improve care for patients. We thus took an interest in the three groups of diseases most frequently responsible for an inflammatory syndrome, infections, cancers and auto-immune diseases. To achieve this, various methods will be used.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Mar 2010
Typical duration for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
March 1, 2010
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 1, 2011
CompletedStudy Completion
Last participant's last visit for all outcomes
February 1, 2012
CompletedFirst Submitted
Initial submission to the registry
July 17, 2013
CompletedFirst Posted
Study publicly available on registry
July 19, 2013
CompletedJuly 19, 2013
July 1, 2013
10 months
July 17, 2013
July 17, 2013
Conditions
Outcome Measures
Primary Outcomes (1)
determination of usual parameters of inflammation
at baseline
Study Arms (1)
Patients with inflammatory syndrome
OTHERInterventions
Eligibility Criteria
You may qualify if:
- Patients presenting an inflammatory syndrome, defined by elevated C-reactive protein (CRP\>50mg/L), whose etiology is related to infection, cancer or an inflammatory disease.
- Age: 18-90 years
- Patients covered by the National Health Insurance Agency
- signed written informed consent form
You may not qualify if:
- Pregnant patients
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
CHU de Dijon
Dijon, 21079, France
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
July 17, 2013
First Posted
July 19, 2013
Study Start
March 1, 2010
Primary Completion
January 1, 2011
Study Completion
February 1, 2012
Last Updated
July 19, 2013
Record last verified: 2013-07