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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05971615
Other study ID # 17-076
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 15, 2020
Est. completion date December 18, 2020

Study information

Verified date July 2023
Source University Hospital, Caen
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

concordance between the lactate values on peripheral venous and arterial blood gases in all patients receiving an arterial sample on their arrival in the S.A.U.V.


Recruitment information / eligibility

Status Completed
Enrollment 90
Est. completion date December 18, 2020
Est. primary completion date December 18, 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria: - one of this condition in emergency unit : 1. acute respiratory distress 2. a suspicion of an acid-base disorder 3. a state of shock 4. Pathologies requiring monitoring of the respiratory system 5. Patient under NIV 6. Poisoning 7. Coma with a Glasgow score < or equal to 8 Exclusion Criteria: - Patient presenting another pathology supported in SAUV not requiring the realization of arterial blood gases - Patient aged < 18 years - Pregnant or breastfeeding woman

Study Design


Related Conditions & MeSH terms


Intervention

Other:
peripheral venous blood gases
peripheral venous blood gases

Locations

Country Name City State
France CAEN University Hospital Caen

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Caen

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary lactates on peripheral venous and arterial blood gases mmol/L baseline
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