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Methods of establishing intersegmental plane in segmentectomy: a prospective randomized controlled study

Methods of establishing intersegmental plane in segmentectomy: a prospective randomized controlled study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300075374
Enrollment
Unknown
Registered
2023-09-03
Start date
2023-09-01
Completion date
Unknown
Last updated
2023-09-11

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

Conditions

Early stage lung cancer

Interventions

1:Closed insufflation technique
2:Dilatation and collapse technique

Sponsors

Second Xiangya Hospital of Central South University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Patients voluntarily join and sign a written informed consent; 2. The age of the subjects is 18-75 years old, regardless of gender; 3. The ECOG PS was 0 or 1; 4. Three-dimensional visualization was performed before surgery, and the surgeon judged that the tumor could be completely removed by segmentectomy, and surgical margin was expected to be greater than 2cm or the maximum diameter of the nodule; 5. Thin-slice CT suggests any of the following: ? The diameter of pulmonary nodules is 2-3cm and the consolidation-tumor ratio (CTR) is less than 0.25; ? Pulmonary nodule diameter =2cm and 0.25 < CTR < 0.5; ? Non-peripheral pulmonary nodule diameter =2cm and CTR=0.25; 6. cN0 and no distant metastasis; 7. Intraoperative freezing examination or postoperative paraffin examination suggest early lung adenocarcinoma; 8. Intraoperative freezing disease of station 12 lymph nodes showed no cancer metastasis; 9. Preoperative anesthesia risk assessment: American Society of Anesthesiologists (ASA) Level I-III; 10. Has no history of lung resection; 11. Has not received anti-tumor therapy such as radiotherapy, chemotherapy, targeted therapy and immunotherapy.

Exclusion criteria

Exclusion criteria: 1. The subject did not understand the study protocol, did not cooperate or refused to sign the informed consent; 2. The subject has a history of malignant tumor or has previously received anti-tumor therapy; 3. 3D visualization was not received before surgery; 4. The surgeon judged that segmentectomy could not ensure complete resection of the tumor; 5. has a history of lung resection, or chest trauma or surgery on the affected side of chest cavity; 6. Extensive intraoperative dense thoracic adhesion; 7. Conversion to thoracotomy; 8. Intraoperative frozen examination of intrapulmonary lymph nodes indicated cancer metastasis; 9. Pulmonary nodules are located in the right middle lung; 10. Suffered from chronic bronchitis, emphysema, asthma and other chronic lung diseases; 11. Other conditions unsuitable for inclusion in this study deemed by the researcher.

Design outcomes

Primary

MeasureTime frame
Intersegmental plane clarity grading;Time of operation for segmentectomy;Postoperative pulmonary function;

Secondary

MeasureTime frame
Minimum distance between the nodule and each margin;The estimated amount of blood loss during the operation;Postoperative days for thoracic drainage;Postoperative hospital stay;

Countries

China

Contacts

Public ContactLiu WenLiang

Department of Thoracic Surgery, Second Xiangya Hospital of Central South University

liuwenliang@csu.edu.cn+86 135 0743 8708

Outcome results

None listed

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