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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02620657
Other study ID # 11224
Secondary ID
Status Completed
Phase
First received
Last updated
Start date December 2015
Est. completion date November 8, 2017

Study information

Verified date August 2019
Source Guangdong Association of Clinical Trials
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

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


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.


Recruitment information / eligibility

Status Completed
Enrollment 2809
Est. completion date November 8, 2017
Est. primary completion date November 8, 2017
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility 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.

Study Design


Intervention

Other:
Non interventional study
Non interventional study

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
ying cheng

Outcome

Type Measure Description Time frame Safety issue
Primary To investigate the proportion of advanced NSCLC patients who performed EGFR mutation test 2014.01.01-2014.12.31
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