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Clinical Trials/NCT02620657
NCT02620657
Completed
Not Applicable

A Retrospective Study on Real-world EGFR Mutation Testing Practice Status and Impact Factors in Patients With Advanced NSCLC in North China

ying cheng0 sites2,809 target enrollmentDecember 2015

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Non-Small Cell Lung Cancer
Sponsor
ying cheng
Enrollment
2809
Primary Endpoint
To investigate the proportion of advanced NSCLC patients who performed EGFR mutation test
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

Approximately 3000 advanced NSCLC patients, who fulfil the inclusion/exclusion criteria, will be recruited by 30 sites in North China.

Detailed Description

Approximately 3000 advanced NSCLC patients will be recruited , and the medical information of recruited patients must be recorded in the hospital electronic system from Jan 1st 2014 to Dec 31st 2014 .The study will focus on the EGFR testing rate in adenocarcinoma patients,so the collecting data for non-adenocarcinoma patients will be controlled in less than 10% for each site.

Registry
clinicaltrials.gov
Start Date
December 2015
End Date
November 8, 2017
Last Updated
6 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
ying cheng
Responsible Party
Sponsor Investigator
Principal Investigator

ying cheng

Director of Jilin Cancer Hospital

Guangdong Association of Clinical Trials

Eligibility Criteria

Inclusion Criteria

  • Histological or cytological confirmed NSCLC;
  • Patients were diagnosed with advanced NSCLC from Jan 1st 2014 to Dec 31st 2014;
  • Researchers should collect the records of consecutive NSCLC patients in each site.

Exclusion Criteria

  • Any patients without NSCLC diagnosis;
  • Any patients which were diagnosed with advanced NSCLC before Jan 1st 2014 or after Dec 31st 2014.

Outcomes

Primary Outcomes

To investigate the proportion of advanced NSCLC patients who performed EGFR mutation test

Time Frame: 2014.01.01-2014.12.31

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