- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00745160
Survey and Blood Sample Collection for Patients With Lung Cancer Who Never Smoked Cigarettes
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
New Jersey
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Basking Ridge, New Jersey, United States
- Memoral Sloan Kettering Cancer Center
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New York
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Commack, New York, United States, 11725
- Memorial Sloan-Kettering Cancer Center @ Suffolk
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New York, New York, United States, 10065
- Memorial Sloan-Kettering Cancer Center
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Rockville Centre, New York, United States, 11570
- Memorial Sloan-Kettering Cancer Center at Mercy Medical Center
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Sleepy Hollow, New York, United States
- Memoral Sloan Kettering Cancer Center@Phelps
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Never-smokers with lung cancer
Internet recruitment The study will be advertised through a specifically designed website linked to the MSKCC Lung Cancer webpage. The website will be designed after approval of the study. The website will be accordingly reviewed by the IRB. We plan to advertise this study by word-of mouth at scientific meetings and on patient associations' websites and/or bulletins, with permission. The website will post a description of the study and an invitation to participate.
Interested patients will be given an email or mail address and/or phone number 866-854-4652 to contact MSKCC investigators about the study.
Description
Inclusion Criteria:
- 18 years or older
- histologically and/or cytologically proven diagnosis of non-small cell lung cancer
- never smoker, defined as having smoked less than 100 cigarettes over one's life-time
- completed survey and inclusion form
- signed informed consent
Exclusion Criteria:
- previous history of cancer (other than lung cancer)
- living outside the United States
- patients who cannot read English (as website and questionnaires will only be written in English)
- unable to understand the protocol or to give informed consent
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
1
Never-smokers with lung cancer
|
After giving informed consent, all patients will be asked to complete questionnaire and will be asked to provide a blood sample for DNA analysis.
The questionnaire will consist of a detailed smoking questionnaire, based on the most recent Centers for Disease Control and Prevention (CDC) Behavioral Risk Factor Surveillance System Survey Questionnaire.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
To assess the feasibility of an internet-based protocol to collect clinical information and biological specimens from 2,000 never smokers with lung cancer.
Time Frame: conclusion of the study
|
conclusion of the study
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Collaborators and Investigators
Investigators
- Principal Investigator: Vincent Miller, MD, Memorial Sloan Kettering Cancer Center
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
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
- 08-104
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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