Trial Outcomes & Findings for Change In Diaphragmatic Thickness Predicts Extubation Success (NCT NCT02656199)
NCT ID: NCT02656199
Last Updated: 2020-03-09
Results Overview
Discontinuation from mechanical ventilation in 48 hours from ultrasound PI has left the institution. Efforts made to contact the PI were unsuccessful. No study data available.
TERMINATED
57 participants
48 hours
2020-03-09
Participant Flow
0 participants analyzed. PI has left the institution. Efforts made to contact the PI were unsuccessful. No study data available.
0 participants analyzed. PI has left the institution. Efforts made to contact the PI were unsuccessful. No study data available.
Participant milestones
| Measure |
Main Cohort
all patients enrolled will have an ultrasound of their diaphragm performed once they are on a pressure support trial. Intervention: Diaphragm Ultrasound
Diaphragm Ultrasound: Once on a pressure support weaning trial, enrolled subjects will have an ultrasound of their right hemidiaphragm performed on three levels of pressure support: 15/5 10/5 and 5/5
0 participants analyzed. PI has left the institution. Efforts made to contact the PI were unsuccessful. No study data available.
PI has left the institution. Efforts made to contact the PI were unsuccessful. No study data available.
|
|---|---|
|
Overall Study
STARTED
|
0
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|
Overall Study
COMPLETED
|
0
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Overall Study
NOT COMPLETED
|
0
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Reasons for withdrawal
Withdrawal data not reported
Baseline Characteristics
Change In Diaphragmatic Thickness Predicts Extubation Success
Baseline characteristics by cohort
Baseline data not reported
PRIMARY outcome
Timeframe: 48 hoursPopulation: PI has left the institution. Efforts made to contact the PI were unsuccessful. No study data available.
Discontinuation from mechanical ventilation in 48 hours from ultrasound PI has left the institution. Efforts made to contact the PI were unsuccessful. No study data available.
Outcome measures
Outcome data not reported
SECONDARY outcome
Timeframe: 48 hours from removal of ventilatory supportReinstitution of mechanical ventilation within 48 hours of extubation PI has left the institution. Efforts made to contact the PI were unsuccessful. No study data available.
Outcome measures
Outcome data not reported
Adverse Events
Main Cohort
Serious adverse events
Adverse event data not reported
Other adverse events
Adverse event data not reported
Additional Information
Roberta Costello; Research Compliance
Albert Einstein Healthcare Network
Results disclosure agreements
- Principal investigator is a sponsor employee
- Publication restrictions are in place