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Characterization of Weaning Practices in ICUs of Global South Countries

H

Hospital do Coracao

Status

Not yet enrolling

Conditions

Weaning Failure
Weaning From Mechanical Ventilation
Weaning From Mechanical Ventilation, Extubation

Study type

Observational

Funder types

Other

Identifiers

NCT07337408
GS Wean - Observational

Details and patient eligibility

About

This is a prospective observational study to be conducted in intensive care units of Global South countries. Patients on mechanical ventilation for more than 12 hours who have initiated the weaning process and for whom the attending team plans extubation within the next 6 hours will be included. Data will be collected for each patient during the first 7 days after extubation, with follow-up until hospital discharge or death. We plan to conduct the study in intensive care units from Global South countries (low- and middle-income countries predominantly located in the Southern Hemisphere, though some in the Northern Hemisphere are also considered).

Enrollment

900 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age > 18 years.
  • Receiving care at an intensive care unit.
  • Endotracheal intubation.
  • Mechanical ventilation for 12 hours or more.
  • First separation attempt, as defined in the WIND Classification - "Separation attempt from mechanical ventilation: an spontaneous breathing trial with or without extubation, or an extubation directly performed without identified spontaneous breathing trial (whatever the type: planned or unplanned extubation)" - planned to occur in the next 6 hours or that occurred less than 2 hours ago.

Exclusion criteria

  • Patients with prior extubation failure.
  • Patients with prior spontaneous breathing trial failure.
  • Patients unable to obey commands.
  • Neuromuscular disease or cervical spinal cord injury.
  • Tracheostomy.
  • Do-not-resuscitate order or contraindication for reintubation.
  • Lack of informed consent.
  • Terminal extubation.
  • Previously included in the study.

Trial contacts and locations

0

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Central trial contact

Aline B Pereira

Data sourced from clinicaltrials.gov

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