Skip to main content
Clinical Trials/NCT05912985
NCT05912985
Recruiting
Not Applicable

Comparison of Three Different Oxygenation Strategies Consisting of Nasal Cannula, Modified Nasopharyngeal Cannula and HFNO (High Flow Nasal Oxygen) in Bronchoscopy Procedures Under Sedation

Ankara City Hospital Bilkent1 site in 1 country252 target enrollmentMarch 28, 2023
ConditionsBronchoscopy

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Bronchoscopy
Sponsor
Ankara City Hospital Bilkent
Enrollment
252
Locations
1
Primary Endpoint
desaturation rate during processing
Status
Recruiting
Last Updated
2 years ago

Overview

Brief Summary

The purpose of study aims to determine which of the three different oxygenation strategies, including nasal cannula, modified nasopharyngeal cannula, and HFNO groups, is safer in patients undergoing bronchoscopy under sedation.

Detailed Description

The patients will be evaluated in the anesthesia polyclinic before the procedure, routine preparation will be made, and written informed consent will be obtained. After being informed about the study and potential risks, all patients who gave written informed consent will be enrolled in the study by recording their demographic information after determining whether they are eligible to participate in the study. In addition, STOP-BANG and FRAIL fragility questionnaires will be administered to the patients. Which oxygenation method should be used which patient will be left to the decision of the Anesthesiologist; The oxygenation tools used in the bronchoscopy unit are nasal cannula, modified nasopharyngeal cannula, and HFNO. When the patients are taken to the procedure room, anesthesia management will be applied by the standard working order of the anesthesia clinic. In addition to non-invasive arterial blood pressure monitoring, 5-channel ECG and pulse oximetry, and standard hemodynamic monitoring, Bispectral Index (BIS) monitoring will be performed. During the process, oxygen saturation will be continuously monitored and the lowest value will be recorded. Interventions made in cases of low oxygen saturation will also be recorded. At the end of the procedure, the patient will be taken to the recovery unit after waking up.

Registry
clinicaltrials.gov
Start Date
March 28, 2023
End Date
March 1, 2024
Last Updated
2 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Süleyman Taş

Principal investigator

Ankara City Hospital Bilkent

Eligibility Criteria

Inclusion Criteria

  • All patients undergoing bronchoscopy

Exclusion Criteria

  • Do not have the ability to read, understand and sign the consent form
  • Pregnancy
  • Contraindications to anesthetic drugs
  • Hemodynamically unstable patients
  • Having a peripheral vascular disease
  • Intubated patients
  • Patients with tracheostomy

Outcomes

Primary Outcomes

desaturation rate during processing

Time Frame: during the procedure, an average of 1 hour

desaturation: oxygen saturation falling below 90%. Oxygen saturation was monitored continuously with a pulse oximeter attached to one of the fingers. It was recorded when oxygen saturation dropped to \< 90%.

Secondary Outcomes

  • rate of airway usage during the process(during the procedure, an average of 1 hour)
  • rate of use of the jaw thrust maneuver during the procedure(during the procedure, an average of 1 hour)

Study Sites (1)

Loading locations...

Similar Trials