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The subcutaneous tunneled periareolar approach in lung resection performed through uniportal video-assisted thoracic surgery

The subcutaneous tunneled periareolar approach in lung resection performed through uniportal video-assisted thoracic surgery

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400093792
Enrollment
Unknown
Registered
2024-12-12
Start date
2024-12-15
Completion date
Unknown
Last updated
2024-12-16

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

Conditions

pulmonary nodule

Interventions

Periareolar Approach Group:Subcutaneous tunnel uniportal thoracoscopic-assisted pulmonary resection via periareolar incision
Traditional Surgical Approaches Group:Intercostal Uniportal/Multipoctal Thoracoscopic-Assisted Pulmonary Resection

Sponsors

DepartmeWest China Hospital of Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1.Diagnosed with a pulmonary nodule, with a solid nodule or solid component diameter >8 mm, or a subsolid nodule with a diameter >=6 mm; 2.Able to understand and cooperate with pain assessment using the Visual Analog Scale (VAS); 3.Lesions Not Involving Adjacent Organs or Major Blood Vessels: This study includes only patients undergoing VATS for pulmonary nodule resection. Eligible cases are those with solid nodules or solid components >8 mm, subsolid nodules >=6 mm, or malignant tumors without invasion of adjacent organs or metastasis.

Exclusion criteria

Exclusion criteria: 1.Patients with Severe Systemic Conditions Unable to Tolerate Surgery: presence of severe coagulation disorders or contraindications for surgery, including serious cardiac, pulmonary, hepatic, or renal diseases; 2.Pulmonary nodule has been diagnosed as malignant with distant metastasis; 3.Pulmonary nodule presents with diffuse, multiple distributions; 4.History of conversion to open thoracotomy.

Design outcomes

Primary

MeasureTime frame
Surgical Completion Rate;Postoperative Complication Rate;Operative Time;Intraoperative Blood Loss;Intraoperative Adverse Event Rate;Pain Visual Analog Scale (VAS) Score;Hospitalization after surgery;

Secondary

MeasureTime frame
Postoperative recovery time;Postoperative drainage volume;Reoperation rate;Usage of surgical equipment or materials;

Countries

China

Contacts

Public ContactDong Tian

West China Hospital of Sichuan University

22tiandong@wchscu.com+86 189 8060 5025

Outcome results

None listed

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