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High Flow Nasal Cannula and Diaphragmatic Function

U

Università degli Studi di Ferrara

Status

Completed

Conditions

Postoperative Complications
Diaphragm Injury

Treatments

Device: High flow nasal cannula
Device: Facial mask

Study type

Interventional

Funder types

Other

Identifiers

NCT05532033
HFNCThoracic

Details and patient eligibility

About

Prospective randomized study investigating the effect of postoperative oxygen delivery on diaphragmatic function. Two different modalities of oxygen delivery will be compared: high flow nasal cannula versus standard oxygen therapy with facial mask

Enrollment

116 patients

Sex

All

Ages

18 to 90 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients scheduled for elective thoracic surgery

Exclusion criteria

  • ASA score >3
  • Body mass index > 35 kg/m2
  • History of neuromuscular disease
  • History of thoracic surgery
  • Phrenic nerve paisy

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

116 participants in 2 patient groups

high flow nasal cannula
Experimental group
Description:
Two hours after extubation patients will received high flow nasal cannula oxygenation therapy for 24 hours
Treatment:
Device: High flow nasal cannula
Standard oxygen therapy
Active Comparator group
Description:
Two hours after extubation patients will received standard oxygenation therapy for 24 hours
Treatment:
Device: Facial mask

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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