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NCT07481435: TRiDENT

TRacheostomy in DElphi for iNTensive Care' (TRiDENT)

Not yet recruiting Last updated 18 March 2026
What this trial tests

trial testing Delphi Consensus Process in Delphi Process in 40 participants. Not yet recruiting.

Timeline
1 May 2026
Primary endpoint
1 October 2026
1 December 2026

Quick facts

Lead sponsorUniversita degli Studi di Genova
StatusNot yet recruiting
Study typeOBSERVATIONAL
Enrollment40
Start date1 May 2026
Primary completion1 October 2026
Estimated completion1 December 2026

Drugs / interventions tested

Conditions studied

Sponsor

Universita degli Studi di Genova — full company profile →

Who can join

18 and older, any sex, with Delphi Process or Delphi Study. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The aim of this study is to develop international consensus-based recommendations for tracheostomy care in critically ill patients. Using the Delphi method, the study seeks to identify key practices in post-tracheostomy management, including tube downsizing and decannulation strategies, infection prevention and site care, restoration of communication and swallowing, and the recognition and management of tracheostomy-related complications. By engaging a multidisciplinary panel of international experts involved in tracheostomy care, the study aims to reduce variability in current practice and support the development of standardized, evidence-informed approaches across different clinical settings.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of Delphi Consensus Process

Trials testing the same drug.

Other Universita degli Studi di Genova 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/NCT07481435.

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