Last reviewed · How we verify

NCT03309423

Is Venous to Arterial Conversion (v-TAC) of Blood Gas Reliable in Critical Ill Patients in the ICU?

Status unknown Last updated 13 October 2017
What this trial tests

trial testing venous to arterial conversion (v-TAC) in Respiratory Insufficiency in 50 participants. Status unknown.

Timeline
9 October 2017
Primary endpoint
30 January 2018
30 March 2018

Quick facts

Lead sponsorAalborg University
StatusStatus unknown
Study typeOBSERVATIONAL
Enrollment50
Start date9 October 2017
Primary completion30 January 2018
Estimated completion30 March 2018
Sites1 location across Denmark

Drugs / interventions tested

Conditions studied

Sponsor

Aalborg University

Who can join

Eligibility, any sex, with Respiratory Insufficiency or Metabolic Disease. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Objective: Arterial blood gas (ABG) is essential in the clinical assessment of potential acutely ill patients venous to arterial conversion (v-TAC), a mathematical method, has recently been developed to convert peripheral venous blood gas (VBG) values to arterialized VBG (aVBG) values. The aim of this study is to test the reliability of aVBG compared to ABG in an intensive care unit (ICU) setting. Method: Consecutive patients admitted to the ICU with pH values \<7,35 or \>7,45 are included in this study. Paired ABG and aVBG samples are drawn from patients via arterial catheter, central venous catheter and/or peripheral venous catheter and compared.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Respiratory Insufficiency

Currently open trials in the same condition.

Other Aalborg University trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03309423.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing