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Effect of topical anesthesia with supraglottic and hypoglottic drug endotracheal tube on stress response of tracheal extubation in patients undergoing general anesthesia

Effect of topical anesthesia with supraglottic and hypoglottic drug endotracheal tube on stress response of tracheal extubation in patients undergoing general anesthesia

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200061823
Enrollment
Unknown
Registered
2022-07-03
Start date
2022-06-20
Completion date
Unknown
Last updated
2023-04-03

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

Conditions

Extubation stress response

Interventions

experimental group:Use ordinary endotracheal tube to intubate through visual laryngoscope, and spray 2 ml of 2% lidocaine after exposing glottis
expermental group 1:The drug injection endotracheal tube was intubated through the visual laryngoscope. 2 ml of 2% lidocaine was injected into the upper and lower glottis through the tube immediately
expermental group 2:The drug injection endotracheal tube was intubated through the visual laryngoscope. Immediately after intubation and 5 minutes before the end of the operation, 2 ml of compound bet

Sponsors

Neijiang First People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Patients undergoing tracheal intubation under elective general anesthesia; 2. ASA anesthesia grade I-II; 3. Aged 18-60 years, body mass index (BMI) < 30 kg/m2; 4. The operation time is more than 2 hours, and the catheterization is successful through one operation within 30 s under the visual laryngoscope.

Exclusion criteria

Exclusion criteria: 1. Patients with hypertension, diabetes, coronary heart disease and respiratory diseases in unstable period; 2. Those with throat pain or inflammation before intubation; 3. Those with pharyngeal anatomy and pathological changes; 4. Communication disorder caused by language function defect or consciousness disorder, mental disease and other reasons; 5. Family members or patients do not agree to participate in this study.

Design outcomes

Primary

MeasureTime frame
hemodynamic parameter;cortisol;Riker sedation and agitation score;

Countries

China

Contacts

Public ContactWu Ailing

Neijiang First People's Hospital

619859344@qq.com+86 18683216262

Outcome results

None listed

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