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Role Of Transthoracic Ultrasound in Predicting Post-extubation Distress During Successful Weaning

A

Assiut University

Status

Not yet enrolling

Conditions

Transthoracic US

Treatments

Device: Transthoracic Ultrasound

Study type

Observational

Funder types

Other

Identifiers

NCT06030401
Transthoracic US

Details and patient eligibility

About

-To Assess Value of Transthoracic Ultrasound In Predicting Post-extubation Distress in Respiratory ICU Using Ultrasound Parameters As Diaphragmatic Excursion ,Diaphragmatic,Diaphragmatic Thickness Fraction,Diaphragmatic Thickness.

Full description

Establishing the correct time to extubate mechanically ventilated patients is a crucial issue in the critical care practice. Both premature and delayed extubation prolong the duration of mechanical ventilation and the intensive care unit (ICU) length of stay and increase morbidity and mortality. Therefore, accurate prediction of post-extubation distress and the early diagnosis of the causes responsible for failure of a trial of pressure support ventilation or a trial of totally unsupported respiration are of paramount importance to improve the outcome of mechanically ventilated patients in the ICU.

The Investigators hypothesized that the use of an integrative thoracic ultrasound assessment, encompassing bedside respiratory, and diaphragm sonographic data, could accurately predict post-extubation distress in patients who succeeded in a pressure support ventilation trial. In addition, The Investigators suggest that the use of appropriate analytical methods, that is, machine-learning methods, could permit the evaluation of the specific impact of respiratory and diaphragm sonographic data on the final estimation of a likelihood of post-extubation distress .

Enrollment

51 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients above 18 yrs. old who admitted to respiratory ICU and mechanically ventilated due to chest diseases and passed weaning trials

Exclusion criteria

  • Pregnancy.
  • Neuromuscular disorders.
  • Psychiatric instability.
  • Uncontrolled cardiovascular disease.
  • Tracheostomy.
  • patints with failed weaning trials.
  • Inability to provide informed consent.

Trial contacts and locations

0

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Central trial contact

Rehab Haredy Hassan, Resident Physicion; Maha kamel Ghanem, prof

Data sourced from clinicaltrials.gov

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