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NCT00476632 Clinical Trial

Epidemiology Controls Using Healthy Participants

Healthy Clinical Trial

Official title:
Epidemiology Controls Using Healthy Participants

Clinical Trial Details — Status: Active, not recruiting

Administrative data
NCT number NCT00476632
Other study ID # 2004-0112
Secondary ID P50CA1006325R01C
Status Active, not recruiting
Phase
First received
Last updated
Start date June 2004
Est. completion date June 2019

Study information
Verified date May 2019
Source M.D. Anderson Cancer Center
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The goal of this research study is to identify biologic and lifestyle factors that may increase a person's risk of developing certain types of cancer.

Description:

For this study, you will be asked to complete a personal interview. During the interview, you will be asked questions about your demographics (age, sex, etc.), certain environmental exposures, your medical history, family history, your diet, and your smoking and alcohol use histories. It should take around 50 minutes to complete the interview.

You will also have around 2 ½ tablespoons of blood drawn for special tests. These tests will look for any biologic factors associated with certain cancers. The interview and blood draw will be scheduled at the time and place of your convenience. You will not be informed of the results of any of the testing done with your samples.

There is a possibility that you might be contacted in the future about if researchers need clarification on any of information already collected. You are free to refuse any further participation if you wish.

This is an investigational study. Up to 1,500 participants will take part in this study.

Recruitment information / eligibility
Status Active, not recruiting
Enrollment 1500
Est. completion date June 2019
Est. primary completion date June 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

1. Individuals ages 18 and over with no prior cancer

2. Willing and able to complete an administered questionnaire

3. Willing and able to donate 30 mL of blood

Exclusion Criteria:

1. Individuals with prior cancer

2. Individuals under the age of 18

Study Design

Related Conditions & MeSH terms

Intervention

Behavioral:
• Questionnaire
50 Minute Interview

Locations
Country Name City State
United States University of Texas MD Anderson Cancer Center Houston Texas

Sponsors (3)
Lead Sponsor Collaborator
M.D. Anderson Cancer Center National Cancer Institute (NCI), National Institutes of Health (NIH)

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary To identify biologic and lifestyle factors that may increase a person's risk of developing certain types of cancer. 6 Years
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