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Establishment of Prediction Model for Postoperative Sore Throat

N

Nanjing Medical University

Status

Not yet enrolling

Conditions

Postoperative Sore Throat

Treatments

Other: Observational studies without intervention

Study type

Observational

Funder types

Other

Identifiers

NCT07088224
KY20250624-12

Details and patient eligibility

About

This observational study aims to identify the risk factors associated with postoperative sore throat (POST) and to develop a clinical prediction model for patients undergoing thyroid surgery under general anesthesia. Despite improvements in surgical and anesthetic techniques, POST remains one of the most common complications following thyroidectomy, with an incidence of up to 80%. POST can significantly impact patient comfort, swallowing function, nutritional intake, and recovery quality, leading to prolonged hospitalization and increased healthcare costs.

The etiology of POST is multifactorial, involving intubation-related factors (e.g., endotracheal tube size, cuff pressure), surgery-related factors (e.g., duration of surgery, neck hyperextension), and patient-related factors (e.g., age, sex, smoking history, pre-existing throat symptoms). However, large-scale, systematic studies in the Chinese population remain limited.

With the increasing adoption of Enhanced Recovery After Surgery (ERAS) principles, the accurate identification of modifiable risk factors and early prediction of POST risk are essential for targeted preventive strategies and improved perioperative management. Recent advancements in machine learning and statistical modeling allow for the development of personalized, multifactorial risk assessment tools.

In this study, clinical data from patients undergoing thyroid surgery at Nanjing First Hospital will be collected and analyzed. The primary goal is to identify key preoperative and intraoperative predictors of POST and to establish a multivariable nomogram-based prediction model. Internal validation using bootstrap methods will be performed to evaluate the model's discrimination, calibration, and clinical utility, ultimately supporting evidence-based interventions to improve postoperative outcomes and patient satisfaction.

Enrollment

375 estimated patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

Age ≥ 18 years; Undergoing thyroid surgery under general anesthesia, including both open and endoscopic procedures; Complete postoperative follow-up records available (minimum 48 hours); Accessible and complete surgical and anesthesia records; Provision of written informed consent by the patient or their legally authorized representative;

Exclusion criteria

Failed tracheal intubation or need for emergency tracheotomy during surgery; Reoperation required due to postoperative complications such as bleeding or nerve injury; Severe cardiopulmonary disease (ASA physical status ≥ IV) or long-term use of corticosteroids; Incomplete clinical data;

Trial contacts and locations

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Data sourced from clinicaltrials.gov

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