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OpenTrials
Completed

NCT Number: NCT05971615

Evaluate the Relevance of the Use of Peripheral Venous Blood Gases for the Care of Patients in the S.A.U.V (Vital Emergency Rooms) of the CHU de Caen

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.

Completed

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Key information

Age range

18 year–70 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

CAEN University Hospital

Caen, France

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • one of this condition in emergency unit :
  • acute respiratory distress
  • a suspicion of an acid-base disorder
  • a state of shock
  • Pathologies requiring monitoring of the respiratory system
  • Patient under NIV
  • Poisoning
  • 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

Treatment and study plan

peripheral venous blood gases

Other

peripheral venous blood gases

Primary outcomes

  1. lactates on peripheral venous and arterial blood gases

    Time frame: baseline

    mmol/L

Sponsors and collaborators

Lead sponsor

University Hospital, Caen

Other

Registry information

Acronym: GDS

Important dates

Study start
2020
Primary completion
2020
Study completion
2020
First posted
Aug 2, 2023
Registry last updated
Aug 2, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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