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Clinical Trials/NCT02502695
NCT02502695
Completed
Not Applicable

A Prospective, Observational, Quality Improvement Study to Optimize Care for Lung Cancer Patients Undergoing Video-Assisted Thoracoscopic Surgery (VATS)

Dana-Farber Cancer Institute6 sites in 1 country173 target enrollmentJune 2015
ConditionsLung Cancer

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Lung Cancer
Sponsor
Dana-Farber Cancer Institute
Enrollment
173
Locations
6
Primary Endpoint
Readmissions rates within 30 days of the patient's surgery date
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

This is a research study for participants who have been diagnosed with lung cancer and are receiving VATS (Video Assisted Thoracoscopic Surgery) lobectomy or segmentectomy. The overall objective of this study is to develop a database to collect data on participants who are undergoing VATS lobectomy or segmentectomy for lung cancer.

Detailed Description

This database will be used as for quality improvement purposes. Furthermore, the database will help in collecting data in an organized fashion, which will help the investigators learn more about the details of the workup performed prior to the surgery, during the surgery, peri-operative management and early follow-up. The investigators hope that this database will help to determine a common guideline to perform VATS lobectomy or segmentectomy. By creating a common guideline for future treatment of VATS patients, the investigators predict the efficiency of the process will increase significantly without decreasing, and perhaps even improving, the quality of the procedure.

Registry
clinicaltrials.gov
Start Date
June 2015
End Date
May 2019
Last Updated
6 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Scott J. Swanson, MD

Principal Investigator

Dana-Farber Cancer Institute

Eligibility Criteria

Inclusion Criteria

  • Male and female subjects
  • Age ≥ 18 years
  • Underwent a VATS lobectomy or segmentectomy procedure for lung cancer -- Note: patients with other malignancies are eligible if they have a primary cancer of the lung as defined above

Exclusion Criteria

  • Subjects undergoing thoracotomy lobectomy or segmentectomy for lung cancer
  • Subjects undergoing surgical procedures other than VATS lobectomy or segmentectomy for lung cancer

Outcomes

Primary Outcomes

Readmissions rates within 30 days of the patient's surgery date

Time Frame: 30 Days

Incidence of post-operative complications within 30 days of the patient's surgery date

Time Frame: 30 Days

Total inpatient cost

Time Frame: 30 Days

Secondary Outcomes

  • Difference in readmission rates between the two cohorts(3 years)

Study Sites (6)

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