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NCT07098611: REXs

A New Tool for Extubation Readiness in Mechanically Ventilated Patients: Readiness for EXtubation Score

Recruiting now Last updated 21 January 2026
What this trial tests

trial in Ventilator Weaning in 470 participants. Currently enrolling.

Timeline
15 June 2025
Primary endpoint
30 December 2026
30 December 2026

Quick facts

Lead sponsorMedipol University
StatusRecruiting now
Study typeOBSERVATIONAL
Enrollment470
Start date15 June 2025
Primary completion30 December 2026
Estimated completion30 December 2026
Sites7 locations across Italy, Turkey (Türkiye), Chile, Iran, Egypt, Spain

Conditions studied

Sponsor

Medipol University

Who can join

Adults 18 to 89, any sex, with Ventilator Weaning or Respiration, Artificial. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Liberation from mechanical ventilation involves three steps: weaning, readiness assessment, and extubation. Readiness is determined using clinical criteria such as improvement of the underlying condition, hemodynamic stability, and adequate respiratory effort. Successful extubation is defined as not requiring invasive support within 48 hours. Due to the complexity of ICU patients, various clinical parameters and multi-component scores have been developed to predict extubation success. This study aims to develop and evaluate a multi-component score, the Readiness for EXtubation score (REXs), to predict extubation readiness in ICU patients under invasive mechanical ventilation.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Ventilator Weaning

Currently open trials in the same condition.

Other Medipol University 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/NCT07098611.

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