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HFHO vs CPAP During Thoracic Surgery

NCT03894072 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 28

Last updated 2021-05-21

No results posted yet for this study

Summary

A single institutional cross-over study design to compare between high flow humidified oxygen (HFHO) device versus conventional CPAP for non-ventilated lung during thoracic surgery.

Conditions

  • Hypoxaemia During Surgery
  • Lung Hyperinflation

Interventions

DEVICE

CPAP

Conventional CPAP

DEVICE

HFHO

A device that can provide heated humidified oxygen up to 30-60 liter per minute, FiO2 (fraction of inspired oxygen) 0.21-0.95

Sponsors & Collaborators

  • Mahidol University

    lead OTHER

Principal Investigators

  • Prasert Sawasdiwipachai, MD · Mahidol University

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Max Age
99 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-03-01
Primary Completion
2019-11-30
Completion
2019-11-30

Countries

  • Thailand

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03894072 on ClinicalTrials.gov