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Research on the preoperative application of dexmedetomidine nasal spray in patients undergoing thoracoscopic surgery

Research on the preoperative application of dexmedetomidine hydrochloride nasal spray in patients undergoing thoracoscopic surgery

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400091847
Enrollment
Unknown
Registered
2024-11-05
Start date
2024-11-06
Completion date
Unknown
Last updated
2024-11-11

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

Conditions

Thoracic diseases (mainly lung lesions)

Interventions

Trial group (dexmedetomidine nasal spray group):Nasal spray with dexmedetomidine nasal spray
Control group (0.9 % physiological saline group):Nasal spray with 0.9 % physiological saline

Sponsors

The First Affiliated Hospital of Guangxi Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: A. Patients undergoing elective thoracoscopic surgery B. ASA classification I-III C. Age 18-65 years old, gender-neutral D. BMI: 18-28 kg/m^2 E. Obtaining informed consent from patient and signing the informed consent form

Exclusion criteria

Exclusion criteria: A. Contraindications to central venous puncture placement B. Subjects considered by the investigator to be unsuitable for nasal spray (e.g., severe rhinitis, nasal deformities, etc.) C. Patients with a history of myocardial infarction or unstable angina, heart rate<60 beats/minute, concomitant grade II or greater atrioventricular block, permanent pacemaker implantation, or severecardiac insufficiency D. Patients with a history of ischaemic stroke or transient ischaemic attack E. Abnormal liver and kidney function F. Combined with hypothyroidism G. Patients with comorbid sleep apnoea syndrome or difficult airway possibilities H. Individuals with intellectual retardation, cognitive dysfunction, and mental system disorders I. History of sedative or psychotropic substance abuse J. Allergy to anaesthetic drugs or ingredients relevant to this study K. Pregnant or lactating women

Design outcomes

Primary

MeasureTime frame
Sedation scores (Sedation success rate);Anxiety scores;Haemodynamic changes during double lumen tube intubation;

Secondary

MeasureTime frame
Sleep scores: 1d before surgery, 1d and 2d after surgery ;MMSE scores: 1d before surgery, 1d and 2d after surgery ;Intraoperative anaesthetic and vasoactive drug dosage;Quality of postoperative recovery;

Countries

China

Contacts

Public ContactYanhua Chen

The First Affiliated Hospital of Guangxi Medical University

402009694@qq.com+86 139 7885 8025

Outcome results

None listed

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