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Evaluation of the Efficacy and Safety of Dexmedetomidine Nasal Spray for Preoperative Use in Painless Fiberoptic Bronchoscopy Diagnosis and Treatment

Evaluation of the Efficacy and Safety of Dexmedetomidine Nasal Spray for Preoperative Use in Painless Fiberoptic Bronchoscopy Diagnosis and Treatment

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500108395
Enrollment
Unknown
Registered
2025-08-29
Start date
2025-09-15
Completion date
Unknown
Last updated
2025-09-01

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

Conditions

Lung Diseases

Interventions

Control group:Preoperative normal saline nasal spray
Drug group:Preoperative administration of dexmedetomidine nasal spray.

Sponsors

Qingdao Municipal Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
19 Years to 64 Years

Inclusion criteria

Inclusion criteria: 1: Aged between 18 and 65 years, regardless of gender; 2: Body Mass Index (BMI) between 18 and 30 kg/m^2 3: American Society of Anesthesiologists (ASA) physical status classification I-III. 4: Patients with indications for fiberoptic bronchoscopy requiring non-intubated general anesthesia. 5: Patients informed about the study and who voluntarily sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1: Mallampati classification grade III or higher, indicating predicted difficult intubation. 2: Comorbidities including severe hypertension, severe arrhythmia, unstable angina, recent acute myocardial infarction, or heart failure. 3: Comorbid neurological, muscular, or psychiatric disorders. 4: Long-term abuse of narcotic analgesics, sedatives, or alcohol addiction. 5: History of gastroesophageal reflux disease or gastric retention. 6: Allergy to any anesthetic drugs used in the study. 7: Pregnant or lactating women.

Design outcomes

Primary

MeasureTime frame
Incidence of Coughing Response;

Secondary

MeasureTime frame
Vital Signs Monitoring;Propofol Dosage and Recovery Time:;Incidence of Respiratory Depression;FOB Procedure Time and Recovery Room Time;

Countries

China

Contacts

Public ContactJunchao Liu

Qingdao Municipal Hospital

junchaoliu1205@163.com+86 136 5532 1632

Outcome results

None listed

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