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NOT YET RECRUITING
NCT07880002
NA

Efficacy and Safety of Nasopharyngeal Tube During Sedation

Sponsor: International Peace Maternity and Child Health Hospital

View on ClinicalTrials.gov

Summary

The goal of this randomized controlled study is to determine whether nasopharyngeal tube oxygenation could increase the fraction of inspired oxygen compared with standard oxygen during a sedated procedure with spontaneous breathing. The main question it aims to answer is: • Does nasopharyngeal tube oxygenation deliver higher fraction of inspired oxygen without increasing adverse events, compared with regular nasal cannula during sedation? Researchers will compare nasopharyngeal tube to regular nasal cannula to see if nasopharyngeal tube oxygenation deliver higher fraction of inspired oxygen. Participants will: • Receive regular nasal cannula or nasopharyngeal tube

Official title: A Study on the Efficacy and Safety of Nasopharyngeal Tube During Sedation

Key Details

Gender

FEMALE

Age Range

18 Years - 60 Years

Study Type

INTERVENTIONAL

Enrollment

160

Start Date

2026-10-08

Completion Date

2027-09-30

Last Updated

2026-10-19

Healthy Volunteers

No

Interventions

DEVICE

nasopharyngeal tube

The nasopharyngeal tube is a soft lubricated wire-reinforced tube with an internal diameter of 2.5mm, and an outer diameter of 4 mm.

DEVICE

regular cannula

A regular nasal cannula is a common method to deliver oxygen.