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Clinical Translation and Application of the Compounded Visual Lung Isolation Tube

Clinical Translation and Application of the Compounded Visual Lung Isolation Tube

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500101822
Enrollment
Unknown
Registered
2025-04-30
Start date
2025-05-05
Completion date
Unknown
Last updated
2025-05-05

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

Conditions

Lung isolation

Interventions

Compounded Tube Group:None

Sponsors

Shanghai Pulmonary Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Aged over 18 years; 2. Undergoing thoracotomy or thoracoscopic surgery under general anesthesia; 3. Classified as ASA physical status I–III; 4. Provided written informed consent.

Exclusion criteria

Exclusion criteria: 1. Contraindications to double-lumen tube use, such as abnormal or narrowed airway anatomy, airway injury, or severe bronchospasm; 2. Other contraindications to surgery or anesthesia; 3. Participation in other interventional studies; 4. Refusal to provide written informed consent.

Design outcomes

Primary

MeasureTime frame
Incidence of complication;

Secondary

MeasureTime frame
Dislocation of the tube;Duration of the intubation procedure;Number of intubation attempts;Visual acuity;Secretion status;Time required for complete lung collapse;Lung isolation effectiveness;

Countries

China

Contacts

Public ContactXin Lv

Shanghai Pulmonary Hospital

xinlvg@126.com+86 136 6186 9972

Outcome results

None listed

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