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NCT05674760: ReAcTCO2

ReAcT CO2: A Study to Assess TcCO2 to Guide Acute NIV

Status unknown NA Last updated 6 January 2023
What this trial tests

NA trial testing Trancutaneous CO2 monitoring (using TCM5 device) in Acute Hypercapnic Respiratory Failure in 60 participants. Status unknown.

Timeline
10 February 2023
Primary endpoint
7 February 2024
10 February 2024

Quick facts

Lead sponsorNottingham University Hospitals NHS Trust
PhaseNA
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingsingle
Primary purposehealth services research
Enrollment60
Start date10 February 2023
Primary completion7 February 2024
Estimated completion10 February 2024

Drugs / interventions tested

Conditions studied

Sponsor

Nottingham University Hospitals NHS Trust

Who can join

18 and older, any sex, with Acute Hypercapnic Respiratory Failure. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Arterial blood sampling is needed to monitor carbon dioxide and PH but is often painful. The aim of this study is to determine whether continuous carbon dioxide monitoring with a skin probe reduces the need for arterial blood sampling by at least 30%. The investigators will also study the safety and effectiveness of skin probe monitoring to manage non-invasive ventilation (NIV).

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Acute Hypercapnic Respiratory Failure

Currently open trials in the same condition.

Other Nottingham University Hospitals NHS Trust trials

Trials by the same sponsor.

Verify against primary sources

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/NCT05674760.

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