- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00260871
Genetic Epidemiological Study of Lung Cancer in Taiwan and Clinical Applications
Genetic Epidemiological Study of Lung Cancer in Taiwan and Clinical Applications-focusing on Female Lung Adenocarcinoma (GEFLAC)
Study Overview
Status
Conditions
Detailed Description
This research proposal intends to integrate epidemiologists, biostatisticians, clinicians, molecular biologists/geneticists to identify susceptible genes for lung cancer, especially for female lung adenocarcinoma, and to study the relationship between gene polymorphisms and clinical outcomes of lung cancer patients. Our objective is to find gene markers for developing useful screening tools for the high risk group in order to prevent or early detect lung cancer, especially female lung adenocarcinoma.
The specific aims of this subproject include:
- Establish and maintain the research network that will recruit and follow up the subjects and families for the GEFLAC study; keeping control of the progress of the study.
- Coordinate all the subprojects such as integrating genotyping data with clinical data and environment data.
- Continue to employ the candidate gene approach to examine the contribution of specific genes to the lung cancer.
- Generate genotyping data for candidate genes in the exploring stage and prioritize SNPs of candidate genes for large scale studies.
- Identify susceptible genes/candidate genes to develop multiplex PCR for screening.
Study Type
Enrollment (Anticipated)
Contacts and Locations
Study Locations
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Miaoli county, Taiwan, 350
- Division of Biostatistics and Bioinformatics, NHRI
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- lung adenocarcinoma
Exclusion Criteria:
-
Study Plan
How is the study designed?
Design Details
- Observational Models: Case-Control
- Time Perspectives: Prospective
Collaborators and Investigators
Collaborators
Investigators
- Study Director: Chao Hsiung, PhD, NHRI
Publications and helpful links
Helpful Links
Study record dates
Study Major Dates
Study Start
Primary Completion
Study Completion
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 94LCP005
- 1.DOH-94-TD-G-111-025
- 2.DOH-94-TD-G-111-027
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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