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Clinical Trials in China / NCT07359586
Recruiting Observational

Laryngopharyngeal Injury After Endotracheal Intubation Under General Anesthesia

NCT07359586 · tracked via the Priya Life Science China tracker
Sponsor
Zhejiang University
Phase
Observational
Started
2025-11-01
Last updated
2026-01-22

Condition(s) studied

Gastric CancerHepatic CarcinomaPulmonary CarcinomaPancreatic CarcinomaCholangiocarcinomaThyroid Carcinoma

Study summary

This study retrospectively analyzed patients who underwent tracheal intubation under general anesthesia at the First Affiliated Hospital of Zhejiang University School of Medicine between October 1, 2015, and September 30, 2025, with a focus on issues related to postoperativelaryngopharyngeal complaints. Patients requiring otolaryngological consultation due to postoperative laryngopharyngeal complaints were identified via the case consultation system. Relevant patient data were collected through the Medison Anesthesia Information Management System and electronic medical record system, and telephone follow-up was conducted to assess patient prognosis. The primary outcome measures were the risk factors of postoperative hoarseness, while the secondary outcome measures included the incidence of postoperative hoarseness, the severity of vocal fold injury and its related risk factors. Additionally, the prognosis of patients and its related risk factors were evaluated. This study aims to reduce the incidence of perioperative laryngopharyngeal injury and provide a reference for the optimization of perioperative anesthetic regimens.

Eligibility

Sex
ALL
Min age
Max age
Healthy volunteers
No
Inclusion Criteria: * Patients who underwent general anesthesia with tracheal intubation at the First Affiliated Hospital of Zhejiang University School of Medicine between October 2015 and September 2025 * Patients who required otolaryngological consultation due to laryngopharyngeal complaints (including hoarseness, sore throat, cough, choking on drinking water, etc.) postoperatively * The surgical type was non-otolaryngological surgery Exclusion Criteria: * Patients with a history of laryngopharyngeal lesions (e.g., granuloma, polyp, tumour, vocal cord paralysis * Patients with a preexisting tracheotomy * Patients requiring postoperative tracheotomy * Patients with incomplete medical records * Patients who underwent multiple surgeries but for whom the specific surgical episode responsible for the laryngopharyngeal complaints could not be identified

Primary outcome measure(s)

Trial sites (2)

FacilityCityRegionStatus
he First Affiliated Hospital, Zhejiang University School of Medicine Hangzhou Zhejiang Completed
The First Affiliated Hospital, Zhejiang University School of Medicine Hangzhou Zhejiang Recruiting

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07359586 on ClinicalTrials.gov ↗ ← All trials in China