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NCT05802316: Awake

Awake Tracheal Intubation in Critical Care Patients

Completed Last updated 6 April 2023
What this trial tests

trial testing tracheal intubation using videolaryngoscope with a hyperangulated blade or standard intubation videolaryngoscopy (VL) and direct laryngoscopy (DL) in Videolaryngoscopy in 140 participants. Completed in 3 November 2022.

Timeline
3 January 2020
Primary endpoint
30 April 2022
3 November 2022

Quick facts

Lead sponsorJohannes Gutenberg University Mainz
StatusCompleted
Study typeOBSERVATIONAL
Enrollment140
Start date3 January 2020
Primary completion30 April 2022
Estimated completion3 November 2022
Sites1 location across Germany

Drugs / interventions tested

Conditions studied

Sponsor

Johannes Gutenberg University Mainz

Who can join

16 and older, any sex, with Videolaryngoscopy or Intensive Care Unit Syndrome. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Tracheal intubation in critical care is a high-risk procedure requiring significant expertise and airway strategy modifications, such as awake intubation with video laryngoscope or flexible endoscope intubation. Furthermore, delayed sequence intubation can be used by experts in certain high-risk subgroups. The investigators hypothesise that awake tracheal intubation is associated with a lower incidence of severe adverse events than standard tracheal intubation in critical care patients.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other recruiting trials for Videolaryngoscopy

Currently open trials in the same condition.

Other Johannes Gutenberg University Mainz 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/NCT05802316.

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