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

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

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCTs072200018
Enrollment
48
Registered
2020-06-23
Start date
2023-03-27
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Oral maxillofacial disease

Interventions

NHF equipment with air administration group respiratory management without device group Face mask with oxygen administration group

Sponsors

Ayuse Takao
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

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

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

Design outcomes

Primary

MeasureTime frame
1) Time-weighted average value of tcpO2 (average partial pressure during the observation period) 2) Time-weighted average value of tcpCO2 (average partial pressure during observation period) 3) SpO2 time-weighted average (average oxygen saturation during observation period) 4) respiratory rate time-weighted average (average respiratory rate during observation period) 5) The rate of occurrence of remarkably high CO2 blood serum in which tcpCO2 is 60 mmHg or more (equivalent to PaCO2> 55 mmHg) for 5 minutes or more 6) Incidence rate of moderate hyper CO2 blood with tcpCO2 of 50mmHg or more (equivalent to PaCO2> 45mmHg) 7) SpO2 decreased to 90% or less, requiring oxygen administration

Contacts

Public ContactTakao Ayuse

Nagasaki University Hospital

ayuse@nagasaki-u.ac.jp+81-958197713

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026