About this trial
Thyroid surgery requires smooth emergence from anesthesia to minimize coughing, hemodynamic fluctuations, and agitation during extubation, which may contribute to postoperative complications such as bleeding or cervical hematoma. Dexmedetomidine, a selective α2-adrenergic receptor agonist, has sedative, analgesic-sparing, and sympatholytic properties that may improve anesthetic stability and recovery quality.
This randomized controlled trial aims to evaluate the effectiveness of a continuous perioperative dexmedetomidine regimen initiated at induction of anesthesia and maintained during thyroid surgery.
The study will compare dexmedetomidine combined with standard balanced anesthesia versus standard anesthesia alone in terms of anesthetic requirements and emergence quality.
The primary hypothesis is that perioperative dexmedetomidine administration reduces anesthetic and opioid requirements and improves emergence quality by decreasing coughing during extubation and hemodynamic responses.
Eligibility criteria
Qualifiers
Age 18-65 years.
American Society of Anesthesiologists (ASA) physical status I-III.
Scheduled for elective thyroid surgery (thyroidectomy) under general anesthesia with endotracheal intubation.
Able to understand the study procedures and provide written informed consent.
Disqualifiers
Known hypersensitivity or contraindication to dexmedetomidine or study-related medications.
Clinically significant cardiac conduction abnormality or arrhythmia (e.g., second- or third-degree atrioventricular block without a pacemaker), severe bradyarrhythmia, or unstable cardiovascular disease.
Severe hepatic dysfunction or severe renal failure.
Pregnancy or breastfeeding.
Trial design
Treatments tested in this trial
- Dexmedetomidine
- Standard General Anesthesia
Treatment groups
Sponsors and collaborators
Bach Mai Hospital
Lead sponsor
Hanoi Medical University
Collaborator