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NCT05532033 Clinical Trial

High Flow Nasal Cannula and Diaphragmatic Function

Postoperative Complications Clinical Trial

Official title:
Effect of High Flow Nasal Cannula vs Standard Oxygen Therapy on Diaphragmatic Function After Thoracic Surgery

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT05532033
Other study ID # HFNCThoracic
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date August 9, 2022
Est. completion date October 22, 2023

Study information
Verified date October 2023
Source Università degli Studi di Ferrara
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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

Recruitment information / eligibility
Status Completed
Enrollment 116
Est. completion date October 22, 2023
Est. primary completion date October 15, 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years to 90 Years
Eligibility 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

Study Design

Related Conditions & MeSH terms

Intervention

Device:
• High flow nasal cannula
A device able to delivery high flow oxygen therapy
• Facial mask
standard oxygen therapy

Locations
Country Name City State
Italy Università di Ferrara Ferrara

Sponsors (1)
Lead Sponsor Collaborator
Università degli Studi di Ferrara

Country where clinical trial is conducted

Italy, 

Outcome
Type Measure Description Time frame Safety issue
Other Days without oxygen support 7 days
Primary Incidence of diaphragmatic dysfunction Ultrasound evaluation of diaphragmatic dysfunction 24 hours after surgery
Secondary Postoperative pulmonary complication Incidence of postoperative pulmonary complication 7 days after surgery
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