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Comparison of Different Oxygenation Methods on Hypoxia Tolerance Time in Patients with Respiratory Apnea under General Anesthesia

Comparison of Different Oxygenation Methods on Hypoxia Tolerance Time in Patients with Respiratory Apnea under General Anesthesia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400079779
Enrollment
Unknown
Registered
2024-01-11
Start date
2024-02-01
Completion date
Unknown
Last updated
2024-01-14

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

Conditions

none

Interventions

Nasal oxygen tube group:After induction, administer 10 L/min of oxygen through the nasal oxygen tube
Nasopharyngeal ventilation tract group:After induction, place the nasopharynx airway and administer oxygen at 10L/min
Threaded pipe group:After induction, the threaded tube opens and blows oxygen towards the mouth and nose, providing oxygen at a rate of 10L/min
Control group:Routine mask oxygenation, induction

Sponsors

The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. 18 years old= age = 70 years old; 2. ASA I or II; 3. Improved Mallampati grade I.-III. 4. Basic pulse oxygen saturation = 97%; 5. Elective surgery under general anesthesia; 6. Sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. The patient refuses to participate; 2. ASA Level III and above; 3. Predictable difficult airway; 4. Tooth loss; 5. Head and facial deformities; 6. History of nasopharyngeal surgery or skull base fracture; 7. Nasal polyps or pronounced nasal septum deviation; 8. Body mass index (BMI)> 30 kg/m2; 9. Pregnant patients; 10. Patients with full stomach and Emergency patients; 11. Upper gastrointestinal bleeding; 12. Pulmonary bullae, bronchiopleural fistula, pneumothorax, etc.; 13. Severe cardiopulmonary dysfunction, etc.

Design outcomes

Primary

MeasureTime frame
Mask ventilation stops when exhaling carbon dioxide;The lowest value of oxygen saturation reached after mask ventilation stops;Exhaled carbon dioxide when ventilation begins after intubation;No ventilation safety time (stop mask ventilation until the patient's oxygen saturation drops to 95%);Ventilation begins after intubation until oxygen saturation returns to 100% of the time;

Secondary

MeasureTime frame
Bleeding from the nasal cavity;Tooth damage;sore throat;Hoarse;Oropharyngeal bleeding;Complications associated with endotracheal intubation;

Countries

China

Contacts

Public ContactShangguan Wangning

The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University

sgwning@163.com+86 135 8763 7891

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026