Skip to content

Effect of dexmedetomidine nasal spray on postoperative sore throat in patients with rigid bronchoscopy under general anesthesia

Effect of dexmedetomidine nasal spray on postoperative sore throat in patients with rigid bronchoscopy under general anesthesia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500106396
Enrollment
Unknown
Registered
2025-07-23
Start date
2025-08-10
Completion date
Unknown
Last updated
2025-08-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None

Interventions

Dexmedetomidine group (group D):1.0µg/kg Dex was administered, dexmedetomidine was diluted to 2ml with normal saline, and 1ml was sprayed on each side of the nasal cavity 10 minutes before surgery
Blank control group (group C):10 minutes before surgery, group C was given the same amount of saline nasal spray

Sponsors

The Affiliated Hospital of Xuzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All

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

MeasureTime frame
Incidence and severity of postoperative sore throat;

Secondary

MeasureTime 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

Public ContactLianyi Zhang

The Affiliated Hospital of Xuzhou Medical University

qqlyly@126.com+86 158 9523 8010

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026