Comparing robotic and video-assisted lung surgery techniques
Robotic Versus Video-assisted Lobectomy/Segmentectomy for Lung Surgery
This study is testing whether robotic lung surgery works better and is safer than video-assisted lung surgery for patients needing lung removal.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 800 (estimated) |
| Ages | 18 Years to 85 Years |
| Sex | All |
| Sponsor | The Second Hospital of Shandong University Academic / other |
| Locations | 1 site (Jinan, Shandong) |
| Trial ID | NCT05270616 on ClinicalTrials.gov |
What this trial studies
This study aims to compare the safety and efficacy of robotic-assisted lobectomy/segmentectomy (RAL/S) with video-assisted lobectomy/segmentectomy (VAL/S) for lung resection. The VAL/S approach is further divided into uniport and multiport techniques. By evaluating these two minimally invasive surgical methods, the study seeks to determine which approach offers better outcomes for patients undergoing lung surgery.
Who should consider this trial
Good fit: Ideal candidates for this study are patients with good cardio-pulmonary function who require minimally invasive lobectomy or segmentectomy.
Not a fit: Patients with poor cardio-pulmonary function or those with large tumors or extensive adhesions in the thoracic cavity may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved surgical outcomes and recovery for patients undergoing lung resection.
How similar studies have performed: Other studies have shown promising results with robotic and video-assisted surgical techniques, indicating potential for success in this approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: 1. good cardio- pulmonary function to tolerate surgery; 2. minimaly invasive surgery for lobectomy or segmentectomy or sleeve lobectomy; Exclusion Criteria: 1. cardio- pulmonary function is not good enough to tolerate surgery; 2. huge tumor or extensive adhesion in thoracic cavity.
Where this trial is running
Jinan, Shandong
- The Second Hospital of Shandong University — Jinan, Shandong, China (Recruiting)
Study contacts
- Study coordinator: Xiaogang Zhao
- Email: zhaoxiaogang@sdu.edu.cn
- Phone: +8617660080007
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.