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To observe the effect of THRIVE on preoxygenation during rapid sequential induction in elderly patients

To observe the effect of THRIVE on preoxygenation during rapid sequential induction in elderly patients

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100050184
Enrollment
Unknown
Registered
2021-08-21
Start date
2021-08-20
Completion date
Unknown
Last updated
2022-04-25

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

Conditions

Rapid sequence induction

Interventions

experimental group:Transnasal Humidified Rapid-Insufflation Ventilatory Exchange
control group:Facemask

Sponsors

Nanjing First Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
65 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Patients undergoing endotracheal intubation under rapid sequence induction under general anesthesia; 2. Aged >= 65 years; 3. ASA classification I-III; 3. Mallampati classification I-II; 4. Have a clear sense of THRIVE; 5. Meet ethical requirements.

Exclusion criteria

Exclusion criteria: 1. Patients with suspected or definite difficult airway; 2. Diseases of the central nervous system; 3. Unable to ventilate with face mask; 4. Serious cardiovascular, pulmonary, liver or kidney disease; 5. Patients with abnormal epistaxis and nasopharyngeal space; 6. Patients with moderate or above anemia; 7. BMI>30kg/m2 8. Patients enrolled in other studies within 30 days; 9. Other researchers considered it inappropriate to participate in this study.

Design outcomes

Primary

MeasureTime frame
PaO2 after 5min preoxygenation (T1);Safe apneic time (from the beginning of laryngoscope to the time when SpO2 drops to 95% or the time when safe apneic time reaching 8min);

Secondary

MeasureTime frame
General information and airway assessment;Intubation time;PaCO2?SpO2?HR?MAP after patients entered the room(T0), 5min after preoxygenation (T1), immediately after successful intubation (T2), safe apniec time reached 8 min or SpO2 decreased to 95%(T3);Manual assisted respiration and use of vasoactive drugs;Cough, reflux, aspiration, aspiration pneumonia and other complications after anesthesia induction;The number of cases with safe apneic time reached 8 min and SpO2>=95%;First mechanical ventilation PETCO2 after intubatio;Minimum SpO2 after facemask ventilation ceases;PaO2 after patients entered the room(T0), immediately after successful intubation (T2), safe apniec time reached 8 min or SpO2 decreased to 95%(T3);

Countries

China

Contacts

Public ContactWang Xiaoliang

Nanjing First Hospital

wxl145381@163.com+86 13776615743

Outcome results

None listed

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