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Clinical Trials/NCT02544477
NCT02544477
Completed
N/A

High-flow Nasal Cannula Oxygen Versus Conventional Oxygen Therapy After Pulmonary Lobectomy

Catholic University of the Sacred Heart1 site in 1 country94 target enrollmentAugust 2015

Overview

Phase
N/A
Intervention
Not specified
Conditions
Respiratory Insufficiency
Sponsor
Catholic University of the Sacred Heart
Enrollment
94
Locations
1
Primary Endpoint
Number of patients with hypoxemia (defined as a PaO2/FiO2 ratio <300) after pulmonary lobectomy in patients with lung cancer
Status
Completed
Last Updated
7 years ago

Overview

Brief Summary

The primary objective of this study is to evaluate the effect of early application of nasal high flow oxygen therapy after pulmonary lobectomy on the incidence of postoperative hypoxemia

Detailed Description

High-flow nasal cannula oxygen (HFNCO) treatment has been showed to have several clinical advantages compared with conventional oxygen therapy. Currently, no reports have described the effects of HFNCO in postoperative patients after thoracic surgery. The primary objective of this study is to determine the incidence of postoperative hypoxemia (defined as a PaO2/FiO2 ratio \<300) in patients with lung cancer after pulmonary lobectomy. In the postoperative period after extubation, patients will be randomly assigned to either: 1. standard oxygen therapy group (control group) or 2. HFNCO group (study group). In the control group, patients will receive oxygen treatment by means of a conventional face mask, with a level of fraction of inspired oxygen (FiO2) set to maintain peripheral oxygen saturation (SpO2) = 92% - 98%. Patients in the study group will be given HFNCO treatment with a gas flow level = 50 L/min and a FiO2 set to maintain peripheral oxygen saturation (SpO2) = 92% - 98%. After 48 hours from study entry, all patients will be evaluated for possible interruption of oxygen treatment on the basis of their clinical conditions.

Registry
clinicaltrials.gov
Start Date
August 2015
End Date
September 2018
Last Updated
7 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Maria Teresa Congedo

Medical Doctor

Catholic University of the Sacred Heart

Eligibility Criteria

Inclusion Criteria

  • planned pulmonary lobectomy for lung cancer

Exclusion Criteria

  • age \<18 years
  • patient refusal
  • body mass index ≥35 kg/m2
  • sleep apnea syndrome
  • tracheostomy
  • home oxygen therapy
  • pregnancy

Outcomes

Primary Outcomes

Number of patients with hypoxemia (defined as a PaO2/FiO2 ratio <300) after pulmonary lobectomy in patients with lung cancer

Time Frame: during the first 96 hours after surgery

Secondary Outcomes

  • Number of patients with SpO2 <93% in room air(after 48 hours from surgery and until 7th post operative day)
  • Postoperative pulmonary complications(during the first 7 days after surgery)
  • Respiratory discomfort evaluated by VAS (visual analogic scale) ranging from 0 (no discomfort) to 10 (maximum imaginable discomfort)(during the first 96 hours after surgery)
  • Number of patients undergoing endotracheal intubation or non-invasive ventilation for acute respiratory failure(during the first 7 days after surgery)

Study Sites (1)

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