ClinicalTrials.Veeva

Menu

Does Positive Pressure Extubation Reduce Postoperative Desaturation? (EXTUBPOS)

U

University Hospital, Lille

Status

Enrolling

Conditions

Postoperative Complications
Lung Ultrasound Score
Extubation

Treatments

Procedure: positive pressure during extubation procedure

Study type

Interventional

Funder types

Other

Identifiers

NCT05295095
2021_0433
2021-A03064-37 (Other Identifier)

Details and patient eligibility

About

Single-center, prospective, controlled, parallel, randomized, single-blind study comparing the conventional extubation technique to two positive pressure extubation techniques on postoperative desaturations

Full description

Study realise on university hospital on Lille in France. Patients inclusion is prospective and randomised in three groups. First group : extubation is realised with aspiration in tracheal tube during removal tube Second group : extubation is realised without aspiration but with APL valve set to 20cmH20 Third group : extubation is realised without aspiration but with ventilator parameters were set for PSV mode (inspiratory pressure of 10cmH2O and PEEP identical to that administered in the operating room

Enrollment

264 estimated patients

Sex

All

Ages

18 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Visceral or urological surgery
  • Scheduled surgery
  • Surgical or patient requirement: placement of an arterial catheter
  • Supine position
  • Post-surgical extubation scheduled in the operating room
  • Minimum age of 18 years
  • Informed and signed consent

Exclusion criteria

  • Severe obesity (BMI over 35kg/m2)
  • pregnant woman
  • Acute or chronic preoperative respiratory pathology.
  • Sleep apnea syndrome
  • Inability to receive informed information (does not speak, read or understand French)
  • Patient under guardianship or curatorship
  • Lack of social security coverage
  • History of intubation or criteria for difficult intubation or ventilation.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

264 participants in 3 patient groups

control group
No Intervention group
Description:
Classical extubation technique : ETT was removed with continuous endotracheal suction
VSPEP
Experimental group
Description:
ETT was removed with APL valve set to 20cmH2O
Treatment:
Procedure: positive pressure during extubation procedure
VSAIPEP
Experimental group
Description:
ETT removed with ventilator parameters were set for PSV mode (inspiratory pressure of 10cmH2O and PEEP identical to that administered in the operating room
Treatment:
Procedure: positive pressure during extubation procedure

Trial contacts and locations

1

Loading...

Central trial contact

Cédric CIRENEI, MD

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems