Trials / Completed
CompletedNCT03480828
Diaphragm Ultrasound to Predict Weaning Outcomes in Mechanically Ventilated Patients
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 36 (actual)
- Sponsor
- Mongi Slim Hospital · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
This trial enrolled all the adult patients who were mechanically ventilated for more than 48 hours and met all creteria for extubation. Patients who needed reintubation for upper aiway obstruction, neurological or hemodynamic alteration were excluded. The diaphragm ultrasound was performed during spontaneous breathing test or pressure support ventilation trial measuring the dipahragmatic excursion (DE) and the diaphragm thickening fraction (DTF) whithin 24 hours before extubation.
Detailed description
This trial enrolled all the adult patients who were mechanically ventilated for more than 48 hours and met all creteria for extubation. Patients who needed reintubation for upper aiway obstruction, neurological or hemodynamic alteration were excluded. The diaphragm ultrasound was performed during spontaneous breathing test or pressure support ventilation trial measuring the dipahragmatic excursion (DE) and the diaphragm thickening fraction (DTF) whithin 24 hours before extubation. The investigators compared the median values of DE and DTF in the group of successfully extubated patients and the group of patients who needed reintubation. Our study compared the utility of DTF and DE to predict extubation success.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DIAGNOSTIC_TEST | comparaison between DE and DTF in prediction of extubation success | diaphragm ultrasound and measurement of DE and DTF in patients meeting all extubation criteria during spontaneous breathing trial |
Timeline
- Start date
- 2017-04-01
- Primary completion
- 2017-12-31
- Completion
- 2017-12-31
- First posted
- 2018-03-29
- Last updated
- 2018-03-30
Locations
1 site across 1 country: Tunisia
Source: ClinicalTrials.gov record NCT03480828. Inclusion in this directory is not an endorsement.