Comparative study of four airway management methods in video-assisted transthoracic surgery

Status

Active, not recruiting

Phases

Phase 1

Study type

Observational

Source

ChiCTR

Registry ID

ChiCTR2200066180

Enrollment

Unknown

Registered

2022-11-26

Start date

2022-11-29

Completion date

Unknown

Last updated

2023-05-15

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

Conditions

Lung tumor

Interventions

Laryngeal mask for spontaneous breathing group:N/A

Laryngeal mask combined with bronchial blocker group:N/A

double-lumen endobronchial tube group:N/A

Single -lumen tube combined with bronchial blocker group:N/A

Eligibility

Sex/Gender

All

Age

18 Years to 80 Years

Inclusion criteria

Inclusion criteria: The patients were schemed to undergo video-assisted transthoracic surgery in general anesthesia for treatment of lung cancer,and ASA class I - III.

Exclusion criteria

Exclusion criteria: Contraindications of pulmonary sequestration; Severe cardiopulmonary insufficiency; A second operation or transfer was planned within 7 days after surgery; Patients with severe liver and kidney dysfunction were not included in this study.

Design outcomes

Primary

Measure	Time frame
Hemameba;Neutrophils;CRP;CRP;Procalcitonin;Postoperative adverse reactions;	—

Secondary

Measure	Time frame
Intraoperative hemodynamic parameters;Length of hospital stay;cost;Intraoperative intake and output volume;surgery duration;Time of anesthesia recovery;Time of anesthesia recovery;Time of anesthesia recovery;	—

Countries

China

Contacts

Public ContactYanhua Luo

55358645@qq.com+86 159 6403 7909

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 9, 2026