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NCT00835809 Clinical Trial

Multi Marker Approach Interest in Emergency in Acute Respiratory Insufficiency Diagnostic

Acute Respiratory Insufficiency Clinical Trial

— BIO-IRA  

Official title:
Multi Marker Approach Interest in Emergency in Acute Respiratory Insufficiency Diagnostic

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00835809
Other study ID # 0811
Secondary ID 2008-A00703-52
Status Completed
Phase N/A
First received February 3, 2009
Last updated September 6, 2010
Start date October 2008
Est. completion date October 2009

Study information
Verified date September 2010
Source University Hospital, Grenoble
Contact n/a
Is FDA regulated No
Health authority France: Afssaps - Agence française de sécurité sanitaire des produits de santé (Saint-Denis)
Study type Observational

Clinical Trial Summary

Biomarkers have an interest in clinic diagnostic ,therapeutic and prognosis in pathophysiologic situation including cardiovascular.But interest of biomarkers in diagnostic care of severe acute respiratory insufficiency remains to clear.

We propose to determine the more relevant marker combination in this case.

Description:

In urgence of a severe acute respiratory insufficiency,for thanks to an approach diagnostic, therapeutic and prognostic we propose to determine the more relevant biomarker combination.

An expert committee will compare the biomarker diagnostic and prognostic relevance thanks to all elements clinico-biological and patient monitoring.

Recruitment information / eligibility
Status Completed
Enrollment 400
Est. completion date October 2009
Est. primary completion date October 2009
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Oxygen saturation below or equal to 92% in ambient air.

- Respiratory frequence above 25 cycle per minute

Exclusion Criteria:

- Minors

- Pregnant or lactating women

- Patient without social security

- Patient hospitalize without consent

- Chest pain with acute coronary electro-cardiographic change leading immediate achievement of a diagnostic coronary angiography and/or therapeutic

- Pneumothorax

Study Design

Observational Model: Cohort, Time Perspective: Prospective

Related Conditions & MeSH terms

Locations
Country Name City State
France University Hospital Grenoble Grenoble

Sponsors (2)
Lead Sponsor Collaborator
University Hospital, Grenoble Regional Clinical Research

Country where clinical trial is conducted

France, 

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