NCT00835809

Brief 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.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
400

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Oct 2008

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

October 1, 2008

Completed
4 months until next milestone

First Submitted

Initial submission to the registry

February 3, 2009

Completed
1 day until next milestone

First Posted

Study publicly available on registry

February 4, 2009

Completed
8 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 1, 2009

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

October 1, 2009

Completed
Last Updated

September 8, 2010

Status Verified

September 1, 2010

Enrollment Period

1 year

First QC Date

February 3, 2009

Last Update Submit

September 6, 2010

Conditions

Acute Respiratory Insufficiency

Keywords

Acute respiratory insufficiency respiratoryBiomarkersEmergencyIntensive care unitProspectivePatient hospitalize in emergency or in intensive care unitfor acute respiratory insufficiency

Study Arms (1)

Acute respiratory diseases.

Patient admit in emergency or intensive care unite with acute respiratory insufficiency.

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Emergency and unit intensive care patient.

You may qualify if:

  • Oxygen saturation below or equal to 92% in ambient air.
  • Respiratory frequence above 25 cycle per minute

You may not qualify if:

  • 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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University Hospital Grenoble

Grenoble, Grenoble, 38000, France

Location

Biospecimen

Retention: SAMPLES WITH DNA

Protein sample

MeSH Terms

Conditions

Emergencies

Condition Hierarchy (Ancestors)

Disease AttributesPathologic ProcessesPathological Conditions, Signs and Symptoms

Study Officials

  • ARA SOMOHANO Claire, PH

    Emergency NGO Onlus

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER

Study Record Dates

First Submitted

February 3, 2009

First Posted

February 4, 2009

Study Start

October 1, 2008

Primary Completion

October 1, 2009

Study Completion

October 1, 2009

Last Updated

September 8, 2010

Record last verified: 2010-09

Locations

FR(1)