Study of the Proteome and Cytokines During Inflammatory Syndromes of Different Etiologies.

NCT ID: NCT01903642

Last Updated: 2013-07-19

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

TERMINATED

Clinical Phase

NA

Total Enrollment

97 participants

Study Classification

INTERVENTIONAL

Study Start Date

2010-03-31

Study Completion Date

2012-02-29

Brief Summary

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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.

Detailed Description

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Conditions

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Inflammatory Disease

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

SINGLE_GROUP

Blinding Strategy

NONE

Study Groups

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Patients with inflammatory syndrome

Group Type OTHER

proteomic analysis

Intervention Type OTHER

Interventions

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proteomic analysis

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

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.

* Patients not on treatment (corticoids, immunosuppressive drugs) during the 7 days preceding inclusion
* Age: 18-90 years
* Patients covered by the National Health Insurance Agency
* signed written informed consent form

* Pregnant patients
Minimum Eligible Age

18 Years

Maximum Eligible Age

90 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Centre Hospitalier Universitaire Dijon

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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CHU de Dijon

Dijon, , France

Site Status

Countries

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France

Other Identifiers

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Bonnotte PHRC IR 2008

Identifier Type: -

Identifier Source: org_study_id

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