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Observational study of a novel nasopharyngeal airway for painless ultrasound-guided bronchial needle aspiration biopsy (EBUS-TBNA)

Observational study of a novel nasopharyngeal airway for painless ultrasound-guided bronchial needle aspiration biopsy (EBUS-TBNA)

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500096711
Enrollment
Unknown
Registered
2025-02-05
Start date
2025-02-10
Completion date
Unknown
Last updated
2025-02-10

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

Conditions

Lung disease

Interventions

New type of nasopharyngeal airway group:Insert a lubricated laryngeal mask (choose the appropriate model according to the patients weight) and perform mechanical ventilation
Laryngeal mask group:After the patient is unconscious, a new, modified nasopharyngeal airway with lubrication is inserted through the nasal cavity

Sponsors

Zunyi Medical University Affiliated Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1.Patients willing to choose painless ultrasound bronchial needle aspiration biopsy 2.Aged from 18 to 70; 3. American Society of anesthesiologists (ASA) grade I ~ II;Mallampatis grade I ~ II; 4.Body mass index (BMI) ranged from 18 to 35.

Exclusion criteria

Exclusion criteria: 1.Preoperative complications include liver, kidney and other organ dysfunction, abnormal coagulation function, or mental illness 2.Severe respiratory insufficiency 3.There are contraindications for the use of laryngeal mask or expected difficulties in the airway 4.Refusal to participate in this experiment 5.Patients with preoperative neurological and psychiatric disorders and cognitive impairment 6.Craniocerebral injury 7.Cerebrospinal fluid otorhinorrhea 8. Nasal airway obstruction, nasal fracture, obvious deviation of nasal septum 9.There is a high risk of reflux aspiration (such as pregnancy, satiety, gastroesophageal reflux disease, or hiatal hernia 10. Identification/suspicion of abuse or long-term use of anesthetic sedatives and analgesics

Design outcomes

Primary

MeasureTime frame
The incidence of pharyngeal pain in patients after extubation;

Secondary

MeasureTime frame
Induction time;Wake-up time;Extubation time;blood pressure;heart rate;EtCO2;Clinical Recovery Score;modified observer's assessment of alert sedation;adverse reaction;Patient and doctor satisfaction;

Countries

China

Contacts

Public ContactNie Jia

Zunyi Medical University Affiliated Hospital

963414483@qq.com+86 135 1852 3326

Outcome results

None listed

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