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Clinical Trials/NCT03710616
NCT03710616
Unknown
Not Applicable

A Real-world Study to Explore Recurrence/Metastases of the Early-stage (I-IIIA) NSCLC Patients and the Impact Factors of Patient Survivals

The First Affiliated Hospital of Guangzhou Medical University1 site in 1 country700 target enrollmentMarch 24, 2018

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Non-small Cell Lung Cancer
Sponsor
The First Affiliated Hospital of Guangzhou Medical University
Enrollment
700
Locations
1
Primary Endpoint
Disease-free survival rates within the configured observation periods
Last Updated
6 years ago

Overview

Brief Summary

The real-world study was designed to explore recurrence/metastases of the patients with non-small cell lung cancer as measured by patient survivals and the impact factors of patient survivals.

Detailed Description

The trial was designed as a real-world observational study to recruit those patients with pathologically diagnosed early-phase non-small cell lung cancer (NSCLC) who were enrolled in the clinical form 2009 to 2017 and explore recurrence/metastases of the NSCLC patients as measured by patient survivals and the impact factors of patient survivals. The study data on patient demographic characteristics, tumor biological characteristics, and clinicla treatments were collected via a retrospectively review method for evaluation of patient survivals and the relevance of clinical characteristics of the patients and patient survivals.

Registry
clinicaltrials.gov
Start Date
March 24, 2018
End Date
January 1, 2023
Last Updated
6 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
The First Affiliated Hospital of Guangzhou Medical University
Responsible Party
Principal Investigator
Principal Investigator

Jianxing He

Professor

The First Affiliated Hospital of Guangzhou Medical University

Eligibility Criteria

Inclusion Criteria

  • The patients who meet all the following inclusion criteria will be included in the study:
  • The patients who were operated with radical operations of the lung cancer;
  • The patients with clinical I-IIIA staging tumors;
  • The pathologically diagnosed NSCLC patients;

Exclusion Criteria

  • Not be specified;

Outcomes

Primary Outcomes

Disease-free survival rates within the configured observation periods

Time Frame: 2009-2017

Disease-free survival rates within 3-month, 6-month, 1-year, 2-year, and 3-year observation periods;

Secondary Outcomes

  • Disease-free survival rates at the configured locations and observation periods(2009-2017)

Study Sites (1)

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