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Ultrasound-guided bilateral internal superior laryngeal nerve block on postoperative throat sore in patients udergoing tonsillectomy: a randomized controlled trial

Ultrasound-guided bilateral internal superior laryngeal nerve block on postoperative throat sore in patients udergoing tonsillectomy: a randomized controlled trial

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400092129
Enrollment
Unknown
Registered
2024-11-11
Start date
2024-12-07
Completion date
Unknown
Last updated
2024-11-18

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

Conditions

amygdalitis

Interventions

group U:Ultrasound guided bilateral internal branch block of upper laryngeal nerve (0.3% ropivacaine, 2.5ml) was performed, bandages were covered on the puncture site.
Control group:Bandages were covered directly to the same nerve block puncture site as group U without nerve block pucture after operation.

Sponsors

Pidu District people's Hospital,Chengdu
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18-65 years; 2. ASA grade I to II; 3. Scheduled for tonsillectomy under general anesthesia.

Exclusion criteria

Exclusion criteria: local neck lesions, coagulopathy or bleeding tendency, allergic to ropivacaine, history of laryngeal nerve injury, local puncture infection, BMI >= 30 kg/m^2, communication disorders, such as intellectual impairment or associated mental illness.

Design outcomes

Primary

MeasureTime frame
Visual analogue scale , VAS;

Secondary

MeasureTime frame
Cough severity rating;Hoarseness severity rating;Tramadol dosage;

Countries

China

Contacts

Public ContactHongguang Gao

Pidu District People's Hospital

gao830117@163.com+86 189 9036 0127

Outcome results

None listed

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