FindTrial
Sign In

A cross-sectional survey of the incidence of postoperative sore throat in patients undergoing nasotracheal intubation in oral and maxillofacial surgery

A cross-sectional survey of the incidence of postoperative sore throat in patients undergoing nasotracheal intubation in oral and maxillofacial surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400091634
Enrollment
Unknown
Registered
2024-10-31
Start date
2024-11-01
Completion date
Unknown
Last updated
2024-11-04

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

Conditions

postoperative sore throat

Interventions

Group of patients undergoing oral and maxillofacial surgery under general anesthesia with nasotracheal intubation:none

Sponsors

Peking University Hospital of Stomatology
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.be scheduled for oral and maxillofacial surgery under general anesthesia with nasotracheal intubation; 18 years old or more; 2.ASA grade I or II;

Exclusion criteria

Exclusion criteria: 1.history of acute upper respiratory tract infection, airway hyperresponsiveness (e.g., asthma) within the last 2 weeks; 2.surgical site involving the pharynx; 3.cognitive impairment; 4.history of combined vital organ insufficiency or psychiatric disorders; 5.presence of contraindications to or history of allergy to anesthetic drugs;

Design outcomes

Primary

MeasureTime frame
postoperative sore throat score(NRS score);—

Countries

China

Contacts

Public ContactLiu Yun

Peking University Hospital of Stomatology

docsusieliu@hotmail.com+86 10 82195287

Outcome results

None listed

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