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A randomized controlled trial on the positioning effect of new wall-less and conventional right-sided double-lumen bronchial catheters in patients undergoing left thoracoscopic surgery

A randomized controlled trial on the positioning effect of new wall-less and conventional right-sided double-lumen bronchial catheters in patients undergoing left thoracoscopic surgery

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600129633
Enrollment
Unknown
Registered
2026-08-07
Start date
2026-08-13
Completion date
Unknown
Last updated
2026-08-10

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

Conditions

Difficulty in positioning after right-sided double-lumen tube intubation with a narrow safety range

Interventions

E group:Use the new type of double-chamber bronchial catheter without a tube wall
NC group:Use the Covidien right double-lumen bronchial tube

Sponsors

Shanghai Chest Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1.? Aged 18 to 75 years, with ASA classification I to III; 2.? Elective left-sided thoracoscopic surgery (lobectomy, segmentectomy or wedge resection); 3. Preoperative three-dimensional reconstruction of chest CT shows that the distance from the tracheal carina to the distal edge of the opening of the right upper lobe is >= 20mm; 4. Voluntarily sign the informed consent form.?

Exclusion criteria

Exclusion criteria: 1. Preoperative CT shows that the distance from the tracheal carina to the distal edge of the opening of the right upper lobe is < 20mm; 2. Presence of airway anatomical variations (such as tracheal bronchus), tracheal stenosis, airway masses, or a previous history of airway surgery; 3. Anticipated difficult airway (Mallampati grade = III, thyromental distance < 6 cm, etc.); 4. Severe cardiopulmonary dysfunction (LVEF < 40%, FEV1 < 50% of the predicted value); 5. Pregnancy or lactation; 6. Refusal to participate in the study.

Design outcomes

Primary

MeasureTime frame
The success rate of the first exposure after intubation;

Secondary

MeasureTime frame
Intubation time;The number of cases requiring intervention due to inadequate one-lung ventilation;Repositioning time after turning;Arterial blood gas analysis at 30 min after one-lung ventilation: PaO2, PaCO2;Increase rate of peak airway pressure;Incidence of tube displacement?;First positioning time?;

Countries

China

Contacts

Public ContactWu Jingxiang

Shanghai Chest Hospital

wjx1132@163.com+86 21 22200000

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Aug 25, 2026