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Ultrasound-guided superior laryngeal nerve block combined sevoflurane inhalation induction in endotracheal intubation of obese patient undergoing elective surgery: a randomized clinical trial

Ultrasound-guided superior laryngeal nerve block combined sevoflurane inhalation induction in endotracheal intubation of obese patient undergoing elective surgery: a randomized clinical trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300074490
Enrollment
Unknown
Registered
2023-08-08
Start date
2024-01-11
Completion date
Unknown
Last updated
2024-01-22

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

Conditions

Obese patient

Interventions

Group A:Group A subjects were subjected to a modified induction intubation protocol. Airway anaesthesia (ultrasound-guided supraglottic nerve block + cricothyroid puncture) was administered first. Sub
Group B:In group B, subjects underwent rapid sequential induction endotracheal intubation, the patient mask inhaled pure oxygen for pregenation before induction until the exhaled oxygen concentration

Sponsors

Department of Anesthesiology, West China Hospital, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Between the ages of 18 and 65; 2. ASA Level I-III; 3. BMI>35kg/m2; 4. Agree to sign an informed consent form.

Exclusion criteria

Exclusion criteria: 1. Aspirated blood oxygen saturation (SPO2)<90%; 2. Patients who are highly suspected of having difficult airways or have a history of difficult airways before anesthesia and require conscious tracheal intubation; 3. Hemodynamic instability; 4. Pregnant patients; 5. There are contraindications for superior laryngeal nerve block; 6. History of allergy to anesthetics; 7. Patients who plan to be transferred to ICU monitoring with tracheal catheters after surgery; 8. Unable to cooperate with the researcher for any reason (such as intellectual disabilities, emotional instability, etc.); 9. Other factors that should not be included in the study (such as postoperative laryngeal cancer, postoperative laryngeal radiotherapy, patients with coronary heart disease, asthma, etc.).

Design outcomes

Primary

MeasureTime frame
The incidence of hypoxia during the peri-intubation period;

Secondary

MeasureTime frame
Hymodynamics parameters;Intubation time;Intubation difficulty scale (IDS);Minimum oxygen saturation during the peri-intubation period;Rate of successful intubation on the first attempt;Incidence of soar throat;Incidence of hoarseness;Incidence of rescue ventilation;Incidence of aspiration of gastric contents during in tubation;

Countries

China

Contacts

Public ContactYusi Hua

Department of Anesthesiology, West China Hospital, Sichuan University

flower_small6@163.com+86 180 8018 1206

Outcome results

None listed

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