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Application of Visual Laryngoscope combined with Disposcope Endoscope for Double-Lumen Endobronchial Tube Intubation and Positioning

Application of Visual Laryngoscope combined with Disposcope Endoscope for Double-Lumen Endobronchial Tube Intubation and Positioning

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500098416
Enrollment
Unknown
Registered
2025-03-07
Start date
2024-02-21
Completion date
Unknown
Last updated
2025-03-10

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

Conditions

Double-Lumen Endobronchial Tube

Interventions

Group D:Disposcope Endoscope was used in the group D
Group F:Fibreoptic bronchoscopy was used in the group F

Sponsors

The First People’s Hospital of Jining
Lead Sponsor

Eligibility

Sex/Gender
All
Age
25 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Patients scheduled for elective thoracic surgery requiring double-lumen bronchial tube intubation at our hospital; 2. Those who aged 25–75 years, regardless of gender, height 155–180 cm, BMI 18–30 kg/m², ASA I–II; 3. Those who informed consent to participate in this study and voluntary participation; 4. All patients can tolerate left-sided DLT intubation, with no difficult airway, good respiratory, circulatory, and endocrine functions, and no organic lesions in vital organs.

Exclusion criteria

Exclusion criteria: 1. Patients predicted to have difficult endotracheal intubation (those who meet any of the following conditions are predicted to have difficult endotracheal intubation: Mallampati grade III or above; mouth opening <= 3 cm; thyromental distance <= 6 cm; neck flexion <= 80°; upper incisor protrusion); 2. Patients who are predicted to have difficulty with mask ventilation; 3. Those whose preoperative chest CT scans indicate abnormal airway anatomy; 4. Those who have had difficulty with endotracheal intubation during previous surgical anesthesia; 5. Those who had upper respiratory tract infection two weeks before surgery, those with pulmonary dysfunction and excessive sputum; 6. Those who cannot use a left-sided double-lumen endobronchial tube for single-lung ventilation.

Design outcomes

Primary

MeasureTime frame
The intubation and positioning time;the rate of the first successful intubation;the incidences of airway injury;the degree of lung collapse;the Visual Quality ;

Secondary

MeasureTime frame
Utilization rate of FOB during intubation;Hemodynamic changes during intubation;

Countries

China

Contacts

Public ContactDI Meixia

The First People’s Hospital of Jining

mzkdmx@163.com+86 151 6673 2857

Outcome results

None listed

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