Ascertainment of Saliva or Blood Samples For Genetic Epidemiology Studies of Cancer and Aging
NCT ID: NCT00579618
Last Updated: 2017-07-31
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
53 participants
OBSERVATIONAL
2006-09-30
2017-07-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Ascertainment of Peripheral Blood or Saliva Samples for Genetic Epidemiology Studies of Familial Cancers
NCT00579163
Blood Samples From Healthy Volunteers for Genetic Studies in the East Anglia Region of the United Kingdom
NCT00757991
Survey and Blood Sample Collection for Patients With Lung Cancer Who Never Smoked Cigarettes
NCT00745160
Collection of Blood From Healthy Patients, Patients With Benign Disease and Patients With Cancer
NCT05181826
BRCA1 Haploinsufficiency and Gene Expression
NCT00597987
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
COHORT
PROSPECTIVE
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Saliva or Blood samples
Extracting sample of saliva or blood only once.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Subjects will self-identify religion and country of origin of grandparents.
* Volunteers will have (by self report) no history of cancer other than nonmelanoma skin cancer. It is recognized that there may be some errors in self report, however, the literature reports a very low error rate for self reported disease reporting for cancer as assessed by interview.
Exclusion Criteria
60 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Susan G. Komen Breast Cancer Foundation
OTHER
Beth Abraham
UNKNOWN
Gurwin Jewish Nursing & Rehabilitation Center
OTHER
Hebrew Home at Riverdale
OTHER
Jewish Home & Hospital Lifecare System
OTHER
Margaret Tietz Nursing and Rehabilitation Center
OTHER
Metropolitan Jewish Health System
OTHER
Northern Services Group
UNKNOWN
Parker Jewish Institute
UNKNOWN
Lenox Hill Neighborhood House
OTHER
JASA at Temple Emanuel of Parkchester Senior Center
UNKNOWN
Van Cortlandt Village Senior Center
OTHER
Memorial Sloan Kettering Cancer Center
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Kenneth Offit, MD, MPH
Role: PRINCIPAL_INVESTIGATOR
Memorial Sloan Kettering Cancer Center
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Memorial Sloan Kettering Cancer Center
New York, New York, United States
Countries
Review the countries where the study has at least one active or historical site.
Related Links
Access external resources that provide additional context or updates about the study.
Memorial Sloan Kettering Web Site
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
06-102
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.