Modified Video-assisted Thoracoscopic Surgery (VATS) Lobectomy for Early-stage Non-small Cell Lung Cancer (NSCLC)

NCT01337037 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 1000

Last updated 2015-01-27

No results posted yet for this study

Summary

The purpose of this study is to modify the surgical technique of VATS (video-assisted thoracoscopic surgery) lobectomy for early-stage non-small cell lung cancer.

Conditions

Interventions

DEVICE

VATS lobectomy using modified equipments

the procedure of this group is the same with standard VATS lobectomy group.the VATS surgical equipments used in the group are designed according to the experience of chinese lobectomy surgery. All the patent applications of the surgical equipments are granted. proprietor of the patents is Jun Wang, head of Department of Thoracic surgery of people's hospital, peking university. Details of the modified equipments: Lobectomy Equipments Pack (Manufacturer B.J.ZH.F.Panther Medical Equipment Co.,Ltd.) consists of 8 basic surgical equipments, which are crafoord dissecting and ligature forcep, Yankauer suction tube, mixter dissecting and ligature forceps(long),mixter dissecting and ligature forceps(short), atraumatic-grip aorta-aneurysma clamp with toothing De Bakey, De Bakey atraumatic-grip vascular forcep, Bozemann tite grip needle holder, Winter placenta and ovum forcep.

PROCEDURE

VATS lobectomy using less staples

VATS lobectomy with at most 4 staples used, aimed at reduced hospital cost.This procedure is similar with the standard VATS lobectomy procedure without staples limits. The lobar vessels and bronchus are stapled. However, the interlobar fissures should be deal with electronic cautery, harmonic scalpel,or suturing.

PROCEDURE

Standard VATS lobectomy

VATS lobectomy without new equipments and limitation of staples, same with the current procedure of VATS lobectomy performed in thoracic departments of Peking university people's hospital and the Collaborators. All procedures were conducted under general anesthesia with double lumen intubation. The thoracoscope was introduced through 7th or 8th intercostals space on the mid-axillaries line. The 4 cm long utility incision was made on the 4th or 5th intercostals space anterior axillary's line without rib-spreading. A third retraction incision located on the 7th or 8th intercostals space sub-scapular line. The surgeon stands on the ventral side of patient using an electrocautery hook and a suction device through the utility incision. Anatomic lobectomy was performed with systemic mediastinal lymph node dissection for lung cancer patients.

PROCEDURE

Open lobectomy

standard lobectomy procedure by thoracotomy approach

Sponsors & Collaborators

  • Shanghai Zhongshan Hospital

    collaborator OTHER
  • West China Hospital

    collaborator OTHER
  • Sun Yat-sen University

    collaborator OTHER
  • The First Hospital of Jilin University

    collaborator OTHER
  • Central South University

    collaborator OTHER
  • Jiangsu Cancer Institute & Hospital

    collaborator OTHER
  • Beijing Friendship Hospital

    collaborator OTHER
  • Xuanwu Hospital, Beijing

    collaborator OTHER
  • Peking University

    collaborator OTHER
  • Fujian Provincial Hospital

    collaborator OTHER
  • Fuzhou General Hospital

    collaborator OTHER
  • Beijing Haidian Hospital

    collaborator OTHER
  • Fuzhou Pulmonary Hospital of Fujian

    collaborator OTHER
  • Peking University People's Hospital

    lead OTHER

Principal Investigators

  • Jun Wang, MD · Department of Thoracic Surgery, Center for Mini-invasive Thoracic Surgery, People's Hospital, Peking University

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-04-30
Primary Completion
2016-12-31
Completion
2016-12-31

Countries

  • China

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01337037 on ClinicalTrials.gov