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Single-port, Two-port Versus Three-port VATS on Non-small Cell Lung Cancer

Primary Purpose

Lung Neoplasm

Status
Unknown status
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
Three-port pulmonary resection surgery
Single-port or two-port surgery
Sponsored by
Cancer Institute and Hospital, Chinese Academy of Medical Sciences
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Lung Neoplasm focused on measuring VATS, NSCLC, recurrence rate

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • age between 18 and 80 years;
  • cT1-3N0-1M0 diagnosed by chest CT or PET-CT before operation;
  • ECOG PS scores≤2;
  • The patients sign informed consents by themselves.

Exclusion Criteria:

  • Inability to tolerance of tracheal intubation and general anesthesia;
  • ECOG PS scores>2;
  • Severe comorbidities including: Angina occurs in 3 months, uncontrolled hypertension, Congestive heart failure, a history of myocardial infarction in 6 months before admission, severe arrhythmia, severe liver, kidney or other metabolic diseases.

Sites / Locations

  • Cancer Hospital of Chinese Academy of Medical SciencesRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

Three-port pulmonary resection surgery

Single-port or two-port surgery

Arm Description

Treated by traditional video assisted thoracoscopic three-port pulmonary resection in the centers with enough experience in VATS and the volume ≧50 cases each year.

Treated by minimally invasive video assisted thoracoscopic single-port or two-port pulmonary resection in the centers with enough experience in VATS and the volume ≧50 cases each year.

Outcomes

Primary Outcome Measures

Local recurrence
two-year local recurrence rate after surgery

Secondary Outcome Measures

Postoperative respiratory complications
Systematic Classification of Morbidity and Mortality After Thoracic Surgery. Grade I, any complication without need for pharmacologic treatment or other intervention. Grade II, any complication that requires pharmacologic treatment or minor intervention only. Grade III , any complication that requires surgical, radiologic, endoscopic intervention, or multitherapy. Grade IV, any complication requiring intensive care unit management and life support. Grade V, any complication leading to the death of the patient.
Lymph node dissection
During the surgery, lymph node dissection were performed. The number of removed lymph-nodes were recorded according to the postoperative pathological diagnosis, and the stations of the lymph node were recorded according to the International Association for the Study of Lung Cancer (IASLC) Lymph Node Map.
Blood loss
blood loss during the surgery

Full Information

First Posted
December 12, 2016
Last Updated
December 12, 2016
Sponsor
Cancer Institute and Hospital, Chinese Academy of Medical Sciences
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1. Study Identification

Unique Protocol Identification Number
NCT02992353
Brief Title
Single-port, Two-port Versus Three-port VATS on Non-small Cell Lung Cancer
Official Title
Single-port Versus Two-port Versus Three-port Video Assisted Thoracoscopic Pulmonary Resection on Non-small Cell Lung Cancer: a Prospective Randomised Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
December 2016
Overall Recruitment Status
Unknown status
Study Start Date
July 2016 (undefined)
Primary Completion Date
June 2019 (Anticipated)
Study Completion Date
June 2019 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Cancer Institute and Hospital, Chinese Academy of Medical Sciences

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
In china, the incidence and death rate of lung cancer is 48.32 per 100 000 person-years and 39.27 per 100 000 person-years, respectively, the highest in malignant tumor. Surgical operation is still main treatment means to resectable NSCLC. VATS pulmonary resection is performed in clinical operation with the aim of decreasing postoperative complications morbidity. The mechanisms may be due to minimize the inflammation reaction to surgical injury. There are some trials regarding two-port VATS versus three-port VATS versus four-port VATS or single-port VATS versus three-port VATS. However, there is no prospective randomised controlled trial regarding Single-port versus two-port versus three-port video assisted thoracoscopic pulmonary resection on NSCLC. So, we hope to demonstrate that single-port and two-port VATS were feasible and safe through the trial, and we hope the results of our study will provide a high level of clinical evidence for choosing the best operative approach in VATS.
Detailed Description
Introduction: In china, the incidence and death rate of lung cancer is 48.32 per 100 000 person-years and 39.27 per 100 000 person-years, respectively, the highest in malignant tumor. Surgical operation is still main treatment means to resectable NSCLC. VATS pulmonary resection is performed in clinical operation with the aim of decreasing postoperative complications morbidity. The mechanisms may be due to minimize the inflammation reaction to surgical injury. There are some trials regarding two-port VATS versus three-port VATS versus four-port VATS or single-port VATS versus three-port VATS. However, there is no prospective randomised controlled trial regarding Single-port versus two-port versus three-port video assisted thoracoscopic pulmonary resection on NSCLC. So, we hope to demonstrate that single-port and two-port VATS were feasible and safe through the trial, and we hope the results of our study will provide a high level of clinical evidence for choosing the best operative approach in VATS. Methods and analysis: this is a three years prospective randomised controlled trial, which aims to attest the safety and feasibility of simple-port VATS and two-port VATS. Group A, B and C receives single-port VATS, two-port VATS and three-port VATS pulmonary resection respectively. The primary endpoint is postoperative recurrence rate. The secondary endpoints include other postoperative complications morbidity , such as the number and location of lymph nodes dissected、operation time, intraoperative volume of blood loss, hospital stays, hospitalization expenses, quantity of using antalgica, change of pulmonary function. 70 patients are enrolled per group in three years, after adding 10% loss of the sample, 77 patients will be required for each group so a total of 231 patients will be enrolled into the study in the end.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Lung Neoplasm
Keywords
VATS, NSCLC, recurrence rate

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
231 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Three-port pulmonary resection surgery
Arm Type
Active Comparator
Arm Description
Treated by traditional video assisted thoracoscopic three-port pulmonary resection in the centers with enough experience in VATS and the volume ≧50 cases each year.
Arm Title
Single-port or two-port surgery
Arm Type
Active Comparator
Arm Description
Treated by minimally invasive video assisted thoracoscopic single-port or two-port pulmonary resection in the centers with enough experience in VATS and the volume ≧50 cases each year.
Intervention Type
Procedure
Intervention Name(s)
Three-port pulmonary resection surgery
Intervention Description
Three-port pulmonary resection surgery
Intervention Type
Procedure
Intervention Name(s)
Single-port or two-port surgery
Intervention Description
Single-port or two-port pulmonary resection surgery
Primary Outcome Measure Information:
Title
Local recurrence
Description
two-year local recurrence rate after surgery
Time Frame
2 years
Secondary Outcome Measure Information:
Title
Postoperative respiratory complications
Description
Systematic Classification of Morbidity and Mortality After Thoracic Surgery. Grade I, any complication without need for pharmacologic treatment or other intervention. Grade II, any complication that requires pharmacologic treatment or minor intervention only. Grade III , any complication that requires surgical, radiologic, endoscopic intervention, or multitherapy. Grade IV, any complication requiring intensive care unit management and life support. Grade V, any complication leading to the death of the patient.
Time Frame
30 days after surgery
Title
Lymph node dissection
Description
During the surgery, lymph node dissection were performed. The number of removed lymph-nodes were recorded according to the postoperative pathological diagnosis, and the stations of the lymph node were recorded according to the International Association for the Study of Lung Cancer (IASLC) Lymph Node Map.
Time Frame
Intraoperation
Title
Blood loss
Description
blood loss during the surgery
Time Frame
Intraoperation

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: age between 18 and 80 years; cT1-3N0-1M0 diagnosed by chest CT or PET-CT before operation; ECOG PS scores≤2; The patients sign informed consents by themselves. Exclusion Criteria: Inability to tolerance of tracheal intubation and general anesthesia; ECOG PS scores>2; Severe comorbidities including: Angina occurs in 3 months, uncontrolled hypertension, Congestive heart failure, a history of myocardial infarction in 6 months before admission, severe arrhythmia, severe liver, kidney or other metabolic diseases.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Juwei Mu, MD
Phone
8610-87788495
Ext
7140
Email
mujuwei@cicams.ac.cn
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Juwei Mu, MD
Organizational Affiliation
Beijing Municipal Science & Technology Commission
Official's Role
Principal Investigator
Facility Information:
Facility Name
Cancer Hospital of Chinese Academy of Medical Sciences
City
Beijing
State/Province
Beijing
ZIP/Postal Code
110000
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Juwei Mu, MD

12. IPD Sharing Statement

Plan to Share IPD
Undecided

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Single-port, Two-port Versus Three-port VATS on Non-small Cell Lung Cancer

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