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Clinical Trials/KCT0006618
KCT0006618
Completed
未知

Comparison of high flow nasal cannula and conventional nasal cannula during sedation for endoscopic submucosal dissection: a randomized controlled trial

Samsung Medical Center0 sites64 target enrollmentTBD
ConditionsNeoplasms

Overview

Phase
未知
Intervention
Not specified
Conditions
Neoplasms
Sponsor
Samsung Medical Center
Enrollment
64
Status
Completed
Last Updated
4 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
January 20, 2022
Last Updated
4 years ago
Study Type
Interventional Study
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • ASA physical status I to III
  • Patients undergoing endoscopic submucosal dissection

Exclusion Criteria

  • \- Patients under the age of 18
  • \- Patients requiring oxygen therapy
  • \- Patients unable to breathe through the nasal
  • \- Patients with severe impaired coagulation profile or who may have nasal bleeding
  • \- Patients who have developed or worsened congestive heart failure within the last 6 months
  • \- Patients with increased intracranial pressure
  • \- Patients with ASA class IV or higher
  • \- Patients with unstable hemodynamics
  • \- Patients with a history of pneumothorax
  • \- Patients with oral and nasal infections

Outcomes

Primary Outcomes

Not specified

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