None
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Study participants undergoing painless rigid tracheoscopy; 2. Age 18 - 75 years old, gender is not limited; 3. Body mass index (BMI) 18~30 kg/m^2; 4. ASA Grading I- III; 5. Have a clear understanding and voluntarily participate in the study, and have the informed consent form signed by themselves or their family members.
Exclusion criteria
Exclusion criteria: 1. History of dexmedetomidine allergy; 2. Previous heart failure or arrhythmia; 3. History of mental illness; 4. History of reflux esophagitis; History of chronic pharyngitis; Preoperative presence of sore throat, hoarseness, dysphagia, bleeding, or use of anticoagulants; high risk of reflux aspiration; History of oral and pharyngeal surgery or upper respiratory tract infection within 2 weeks before surgery; 5. Abnormal liver and kidney function; 6. Refusal to sign the informed consent form; 7. Recent nasal injury; 8. Has participated in other researchers.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Incidence and severity of postoperative sore throat; | — |
Secondary
| Measure | Time frame |
|---|---|
| Preoperative, intraoperative and postoperative hemodynamic changes were observed;The amount of anesthetics used;The incidence of postoperative nausea and vomiting;Postoperative hoarseness and cough were observed;Quality of postoperative recovery QoR-15 score;Ramsay score in the recovery room;Participant satisfaction and operator satisfaction;Rigid bronchoscope placement time, placement times and indwelling time;; | — |
Countries
China
Contacts
The Affiliated Hospital of Xuzhou Medical University