Comparison of a NaPSflex and Traditional Nasal Cannula During Intravenous Anesthesia for Gastroscopy Procedures: A Randomized Controlled Trial

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2400086626

Enrollment

Unknown

Registered

2024-07-08

Start date

2024-07-10

Completion date

Unknown

Last updated

2024-07-15

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

Conditions

None listed

Interventions

NaPSflex Group:Oxygen is administered using NaPSflex

Nasal cannula Group:Oxygen is administered using a nasal cannula

Eligibility

Sex/Gender

All

Age

18 Years to 100 Years

Inclusion criteria

Inclusion criteria: (1) Endoscopy with intravenous anesthesia (2) Age =18 years old (3) American Society of Anesthesiologists (ASA) Grade ?-? (4) Be able to understand the process and method of this study, and voluntarily participate in this study.

Exclusion criteria

Exclusion criteria: (1) Severe obstructive sleep apnea syndrome; (2) History of severe arrhythmia, acute pharyngitis, tonsillitis; Pneumonia or anaerobic pulse oxygen saturation (SpO2) <90% (3) A history of myocardial infarction and unstable angina pectoris in the last 6 months (4) Pathological changes or surgical history of the nose and throat (5) Allergy to propofol, eggs, soy or albumin (6) Lack of cooperation ability (7) Pregnancy or lactation

Design outcomes

Primary

Measure	Time frame
Incidence of hypoxemia;	—

Secondary

Measure	Time frame
Duration of hypoxemia (s);Severe hypoxemia;minimal pulse oxygen saturation;assisted airway ventilation (Jaw thrust, Mask-assisted ventilation);Increasing oxygen flow;Anesthesiologist satisfaction;	—

Countries

China

Contacts

Public ContactXia Jianhua

Shanghai Pudong New Area People's Hospital

jianhuaxia2000@sina.com+86 136 0180 2789

Outcome results