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Analgesic effect of superior laryngeal nerve block in vocal cord polypus extraction under supporting laryngoscope

Analgesic effect of superior laryngeal nerve block in vocal cord polypus extraction under supporting laryngoscope

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300072463
Enrollment
Unknown
Registered
2023-06-14
Start date
2023-06-15
Completion date
Unknown
Last updated
2023-06-18

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

Conditions

Vocal cord polyp

Interventions

Lidocaine combined with intravenous general anesthesia group:2% lidocaine 3ml spray throat
Superior laryngeal nerve block combined with intravenous general anesthesia group:0.3% ropivacaine 5ml, bilateral superior laryngeal nerve block under ultrasound guidance.

Sponsors

Suining Central Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Patients who plan to undergo vocal cord polyp removal under supportive laryngoscope; Age 18 to 60 years old; ASA Level I or II; The patient has full informed consent, is willing to undergo the experiment, and is eligible for follow-up.

Exclusion criteria

Exclusion criteria: Dementia, impaired cognitive function, central nervous system disorder, peripheral neuropathy, allergy to amide local anesthetics, infection at the puncture site, restricted mouth opening, glaucoma, inability to correctly understand the Prince Henry score, and unsuitable for patients under general anesthesia.

Design outcomes

Primary

MeasureTime frame
Prince-Henry score;patient satisfaction;Hemodynamic values;

Secondary

MeasureTime frame
Adverse reactions;

Countries

China

Contacts

Public ContactYI Liang

Suining Central Hospital

1144137908@qq.com+86 183 9815 4358

Outcome results

None listed

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