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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT03352635
Other study ID # 5P01CA138388-06
Secondary ID
Status Withdrawn
Phase N/A
First received July 25, 2017
Last updated November 17, 2017
Start date September 1, 2017
Est. completion date August 30, 2022

Study information

Verified date November 2017
Source University of Minnesota - Clinical and Translational Science Institute
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The purpose of the study is to collect human biological samples and measurements from people of various ethnic and racial backgrounds for projects related to the "Mechanisms of Ethnic/Racial Differences in Lung Cancer Due to Cigarette Smoking" Program Project Grant. These samples will be used to evaluate and compare biomarkers of tobacco exposure across Japanese Americans, Whites, and Native Hawaiians and to add to the Multiethnic Cohort (MEC) biorepository to develop or assess future biomarkers.


Description:

This cross-sectional, observational study will primarily recruit smokers from the MEC study. The biological samples from these smokers are being collected since they do not currently exist in the biorepository (e.g. buccal cells). Potential smokers from the three racial groups who meet specific inclusion criteria will be invited to participate in the study. Should recruitment from the MEC sample be insufficient, smokers who meet the criteria will be recruited from the general population. This study will involve one to two home visits where tobacco use and medical history and biological samples will be collected including blood, buccal cells and urine.

Approximately 300 smokers will be recruited from the Multiethnic Cohort (MEC) study or the general population in Hawai'i. 100 participants from each of the three designated ethnic/racial groups: Native Hawaiians, Japanese Americans and Non-Hispanic Whites. All participants will be recruited from Hawai'i to reduce variation due to geographical location and maximize ability to recruit the targeted ethnic/racial groups.

This study will involve one to two home visits where demographics, tobacco use and exposure history, medical history and medication use, questionnaires assessing tobacco dependence, alcohol use, and environmental exposures will be administered. and biological samples will be collected including blood, buccal cells and urine.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date August 30, 2022
Est. primary completion date August 30, 2021
Accepts healthy volunteers
Gender All
Age group 21 Years and older
Eligibility Inclusion Criteria:

1. One of the three targeted ethnic groups: 1)Japanese American - two parents of Japanese descent; 2) Non-Hispanic Whites - two parents of non-Hispanic white descent; 3) Native Hawaiians will include individuals with at least one parent of Hawaiian descent;

2. Smoke 5 cigarettes per day over the past three months;

3. >21 years of age;

4. Consumes 14 or fewer drinks of alcohol per week;

5. Generally stable and good health (determined by review of medical history);

6. Able to provide written voluntary consent before performance of any study related procedure.

Exclusion Criteria:

1. Current use of other nicotine containing products for > 4 times per month (and no use of any nicotine-containing products except cigarettes for 2 weeks prior to their study visits);

2. Acute or uncontrolled medical or psychiatric conditions;

3. Currently taking any medications that affect relevant metabolic enzymes or anti- inflammatory medications such as ibuprofen (this will be reviewed by study investigators on a case-by-case basis);

4. Active infection (e.g., influenza, cold, respiratory infection, sinus infection) at the time of the visit;

5. Pregnant or nursing or planning on becoming pregnant during the study;

6. Unable to read and understand English.

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
United States Masonic Cancer Center, University of Minnesota Minneapolis Minnesota
United States Tobacco Research Programs University of Minnesota Minneapolis Minnesota

Sponsors (1)

Lead Sponsor Collaborator
University of Minnesota - Clinical and Translational Science Institute

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Project 3: Analysis of 1,3-butadiene DNA adducts Ethnic differences in butadiene-DNA adducts across racial groups to determine the relationship of DNA adducts to lung cancer and the influence of carcinogen metabolizing genes on DNA adduct formation, repair, and toxicity/mutagenicity. Baseline
Primary Project 4: Correlation of DNA adducts of buccal cells and urinary markers and lung cancer risk DNA adduct levels in oral cells, themselves or together with urinary biomarker levels, correlate with lung cancer risk across various ethnic/racial groups Baseline
Primary Project 2: NNK a-hydroxylation Analysis of biomarkers of NNK a-hydroxylation (bioactivation) pathway and the effect of P450 2A6 activity on this process. Baseline
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