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Starting soon Not applicable

The Effect of Esketamine on Cough Reflex During Tracheal Extubation in Patients Undergoing Non-inflatable Transoral Endoscopic Thyroid Surgery

NCT07641673 · tracked via the Priya Life Science China tracker
Phase
Not applicable
Started
2026-06
Last updated
2026-06-11

Condition(s) studied

ThyroidectomyCoughing Reflex

Investigational drug(s) / intervention(s)

Esketamine(iv) →ESK sprayNormal Saline

Esketamine(iv): During anesthesia induction, administer esketamine intravenously at 0.5 mg/kg. Once muscle relaxation is achieved, under direct laryngoscopic visualization, spray physiological saline (3 ml) above the glottis, at the glottis, and below the glottis.

ESK spray: During anesthesia induction, Once muscle relaxation is achieved, under direct laryngoscopic visualization, spray esketamine at the supraglottic, glottic, and subglottic levels: 3 ml (0.5 mg/kg).

Normal Saline: During anesthesia induction, intravenous injection of an equal amount of normal saline is administered. After achieving muscle relaxation, under direct laryngoscopic view, spray normal saline over the supraglottic, glottic, and subglottic areas: 3 ml.

Study summary

This study intends to implement esketamine-assisted anesthesia in patients undergoing non-inflatable transoral endoscopic thyroidectomy through a prospective randomized controlled trial, in order to observe the effect of esketamine on coughing during extubation in thyroidectomy patients.

Eligibility

Sex
ALL
Min age
18 Years
Max age
65 Years
Healthy volunteers
No
Inclusion Criteria: * Patients scheduled for endotracheal intubation-free thyroid surgery under oral endoscopy * ASA class I-II * Voluntarily participate in the study and sign the informed consent form Exclusion Criteria: * Body Mass Index \> 30 kg/m² * Patients with unstable ischemic cardiomyopathy, pulmonary hypertension, poorly controlled or untreated hypertension (arterial hypertension, resting systolic/diastolic blood pressure \>180/100 mmHg) * Hepatic or renal dysfunction * History of oral, maxillofacial, neck, or airway surgery, or pathological structural alterations * Respiratory diseases (COPD, asthma, inflammation, chronic cough) * Patients with elevated intracranial pressure * Patients undergoing repeat surgery * History of allergy to the investigational drug used in the study * Patients with psychiatric disorders or alcohol abuse (daily ethanol intake ≥40 g, or having experienced alcohol withdrawal within the past 6 months, or unable to control alcohol consumption)

Primary outcome measure(s)

  • Incidence of coughing during tracheal extubation — Perioperative (From the awakening period to immediately after tracheal extubation)
    0=None; 0 = Did not occur; 1 = Occurred;

Trial sites (1)

FacilityCityRegionStatus
Second Affiliated Hospital of Anhui Medical University Hefei Anhui
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 NCT07641673 on ClinicalTrials.gov ↗ ← All trials in China