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HFNC for Induction During Bariatric Surgery Patients.

F

Fundación para la Investigación del Hospital Clínico de Valencia

Status

Completed

Conditions

Lung Collapse

Treatments

Procedure: Standard group
Procedure: HFNC group

Study type

Interventional

Funder types

Other

Identifiers

NCT03155711
HFNC-Obese

Details and patient eligibility

About

This study aims to compared the effects of high flow nasal during the induction and during the weaning of anesthesia on intraoperative and postoperative oxygenation and postoperative atelectasis in obese patients undergoing bariatric surgery versus the standard of care, which consists in supplemental oxygen with face mask (Venturi mask).

Enrollment

64 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Body mass index > 35 Kg/m2
  • Bariatric surgery
  • Informed consent signed

Exclusion criteria

  • age <18yr or >80yr
  • pregnancy or breast-feeding status
  • patients with previous known respiratory disease
  • hemodynamic instability at entry (need of vasopressors or ionotropes at entry or a ventricular assist device

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

64 participants in 2 patient groups

HFNC
Experimental group
Description:
HFNC with a 60 liters per minute flow will be given to the patients before anesthesia induction and before extubation at the end of the surgery
Treatment:
Procedure: HFNC group
Standard
Active Comparator group
Description:
This patients will be managed as usual care. Pre-oxygenation before induction will be performed with supplemental oxygen but without positive pressure. After extubation patients will be oxygenated through a ventury mask.
Treatment:
Procedure: Standard group

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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