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Research on the Application of Ultrasound - Guided Anterior - Approach Superior Laryngeal Nerve Block in Nasotracheal Intubation Guided by Conscious Fiberoptic Bronchoscopy in Patients Undergoing Snoring Surgery

Research on the Application of Ultrasound - Guided Anterior - Approach Superior Laryngeal Nerve Block in Nasotracheal Intubation Guided by Conscious Fiberoptic Bronchoscopy in Patients Undergoing Snoring Surgery

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500113815
Enrollment
Unknown
Registered
2025-12-03
Start date
2026-01-01
Completion date
Unknown
Last updated
2025-12-08

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

Conditions

Sleep Apnea Syndrome

Interventions

Surface anesthesia group:Surface anesthesia of the oropharynx and glottis
Nerve block group:Ultrasound-guided bilateral superior laryngeal nerve block via anterior approach

Sponsors

West China Hospital of Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Aged between 18 and 65; 2. Diagnosis of SAS: The diagnostic criteria for sleep apnea syndrome (SAS) mainly rely on symptoms, signs, and the results of polysomnography (PSG). The core indicator is the occurrence of >=5 apnea or hypopnea events per hour during sleep (AHI >=5 events/hour), accompanied by related symptoms or health risks; 3. Diagnosed with SAS and SAS I–III; 4. Agree to sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1.For any reason, if a subject is unable to cooperate with the research or if the researcher deems it inappropriate for the subject to be included in this trial. 2.Patients with contraindications for awake bronchoscopy intubation (patients who are awake but tense or confused and estimated to be unable to cooperate; patients allergic to local anesthetics; patients with frequent bronchial asthma; patients with active bleeding in the airway and opaque secretions); 3.There are contraindications for superior laryngeal nerve block (infection at the puncture site, cervical mass, allergy to local anesthetics, severe bleeding tendency, and inability to cooperate). 4.Patients with a history of allergy to the drugs involved in this study; 5.Patients with persistent cough and upper respiratory tract infection before surgery; 6.The past medical history includes factors that should not be included in the study (such as patients who have undergone laryngeal cancer surgery, received laryngeal radiotherapy, have coronary heart disease, or suffer from asthma, etc.).

Design outcomes

Primary

MeasureTime frame
Tolerance rate;

Secondary

MeasureTime frame
The time consumption of airway anesthesia;Hemodynamic parameters during the peri-intubation period;One-time intubation success rate;Glottic condition;The subjective satisfaction of intubation doctors;The incidence and severity of coughing during extubation;Subjective discomfort of awake intubation in patients;The incidence of complications;Intubation time;The incidence and severity of intubation coughing;

Countries

China

Contacts

Public ContactChen Guo

West China Hospital of Sichuan University

grace_chenguo@hotmail.com+86 18980601577

Outcome results

None listed

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