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A prospective randomized controlled clinical study of NIVATS on postoperative diaphragm function in patients undergoing single-port thoracoscopic lung occupying resection

A prospective randomized controlled clinical study of NIVATS on postoperative diaphragm function in patients undergoing single-port thoracoscopic lung occupying resection

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200064252
Enrollment
Unknown
Registered
2022-10-01
Start date
2022-10-01
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 cancer

Interventions

Endotracheal intubation group:Endotracheal intubation
NIVATS group:non-intubated

Sponsors

the Second Hospital of Shandong University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Body mass index(BMI) <= 30 kg/m2 2. American Society of Anesthesiologists(ASA) physical status classification score of I to III 3.18 years <= Age <=70 years 4. Patients undergoing single-incision video-assisted thoracoscopic lung resection surgery.

Exclusion criteria

Exclusion criteria: 1. BMI >30 kg/m2 2. ASA> III 3. Age70 years 4. Significant cardiopulmonary insufficiency or with other serious diseases 5. Operation time >5 hours 6. Contraindications to drugs or procedures involved 7. Difficult airway (Mallampati classification >III) 8. Diaphragm dysfunction before surgery or diaphragm images were not available 9. History of thoracic surgery.

Design outcomes

Primary

MeasureTime frame
diaphragmatic function;—

Secondary

MeasureTime frame
pulmonary complications;—

Countries

China

Contacts

Public ContactNing Li

the Second Hospital of Shandong University

lining252252@126.com+86 13791036442

Outcome results

None listed

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