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Application of SEEKFLEX Stylet for Subglottic Ventilation in Flexible Bronchoscopy: A randomized controlled trial

Application of SEEKFLEX Stylet for Subglottic Ventilation in Flexible Bronchoscopy: A randomized controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600120828
Enrollment
Unknown
Registered
2026-03-20
Start date
2026-03-20
Completion date
Unknown
Last updated
2026-03-23

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

Conditions

Airway abnormalities

Interventions

SEEK Core Group (Group S):Adjustable endotracheal intubation kit (SEEKflex tube core) for subglottic ventilation
Double-lumen laryngeal mask Group (Group P):Ventilation through a double-cuff laryngeal mask airway above the glottis

Sponsors

People's Hospital of Pudong New Area, Shanghai
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: (1) Age between 18 and 80 (2) All patients underwent bronchoscopy under general anesthesia, meeting the indications for examination and treatment; (3) Normal speech and comprehension, able to complete the filling of the scale; (4) ASA I-III class; (5) Body Mass Index (BMI) < 30 kg/m^2; (6) The bronchoscopy examination is expected to take less than 30 minutes;

Exclusion criteria

Exclusion criteria: (1) Patients with other nasal diseases; (2) Severe cardiopulmonary insufficiency, arrhythmia, severe hypertension, poorly controlled diabetes, etc; (3) Combined with severe airway stenosis; (4) Patients with severe respiratory failure or severe coagulation dysfunction; (5) Skull base fracture or nasal bone fracture; (6) Refusing to participate in this study or having already participated in other studies;

Design outcomes

Primary

MeasureTime frame
Hypoxaemia;

Secondary

MeasureTime frame
Blood pressure;heart rate;blood gas analysis;Aspiration;Nose bleeding;Tracheal mucosa injury/ hemorrhage;Emergency endotracheal intubation;Bronchospasm;Adverse events related to the sedation;Procedure time;Time to fully alert;Total anaesthetic dose;Subcutaneous emphysema;Gastric insufflation;Patient satisfaction score;Bronchoscopist satisfaction score;

Countries

China

Contacts

Public ContactXia Jianhua

People's Hospital of Pudong New Area, Shanghai

jianhuaxia2000@sina.com+86 136 0180 2789

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Apr 3, 2026