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A study on respiratory management in acute postoperative period by Nasal High Flow for patients undergoing surgery under general anesthesia

Not Applicable
Recruiting
Conditions
Oral maxillofacial disease
Registration Number
JPRN-jRCTs072200018
Lead Sponsor
Ayuse Takao
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
48
Inclusion Criteria

1 Age: Adult patients aged 18 to 85 years of age at the time of consent acquisition
2 Gender: Any question
3 hospitalization / outpatient: hospitalization only
4 Patients who received written consent by their own free will after thorough understanding before participating in this study

Exclusion Criteria

1) Patients who have already been receiving continuous oxygen (home oxygen therapy) by nasal cannula
2) Patients who cannot breathe nose
3) Patients who cannot reduce or discontinue antithrombotic drugs after surgery
4) Patients with a history of pneumothorax
5) Patients who need to administer drugs for pain control after surgery
6) Patients with significant postoperative morphological changes such as extensive resection of the jawbone
7) Other patients judged by the investigator to be inappropriate as study subjects
8) Patients who are positive for the new coronavirus (SARS-CoV-2) PCR test

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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