Clinical Trials Directory

Trials / Terminated

TerminatedNCT00870961

Vitamin D Supplement in Preventing Colon Cancer in African Americans With Colon Polyps

Vitamin D Intervention For Colon Cancer Prevention In African-Americans-A Pilot Study

Status
Terminated
Phase
N/A
Study type
Interventional
Enrollment
22 (actual)
Sponsor
Northwestern University · Academic / Other
Sex
All
Age
50 Years
Healthy volunteers
Not accepted

Summary

RATIONALE: Chemoprevention is the use of certain drugs to keep cancer from forming. The use of vitamin D may keep colorectal cancer from forming in patients with colon polyps. PURPOSE: This randomized phase I trial is studying a vitamin D supplement to see how well it works compared with a placebo in preventing colorectal cancer in African Americans with colon polyps.

Detailed description

OBJECTIVES: Primary * To determine the accrual rate of African Americans with adenomatous polyps to a 6-month randomized intervention trial comprising supplementation with either cholecalciferol (vitamin D3) or placebo. * To determine the compliance rates in patients treated with these regimens. Secondary * To compare changes in pre- and post-treatment vitamin D levels in patients treated with these regimens. * To correlate vitamin D levels with vitamin D modifiers, such as levels of skin pigmentation, dietary vitamin D intake, and sun exposure in this patient population. OUTLINE: Patients are randomized to 1 of 2 arms. * Arm I: Patients receive oral cholecalciferol (vitamin D3) supplementation daily for up to 6 months in the absence of disease progression or unacceptable toxicity. * Arm II: Patients receive oral placebo supplementation daily for up to 6 months in the absence of disease progression or unacceptable toxicity. Patients complete questionnaires about demographics, dietary vitamin D intake, personal history (e.g., ancestry, alcohol and tobacco intake, occupation, height, and weight), medical history (e.g., personal and family history of colorectal cancer and polyps), and ultraviolet radiation exposure. Blood samples are collected at baseline and at 6 months for correlative laboratory studies. Blood samples are analyzed for vitamin D levels by enzyme immunoassay. Patients also undergo assessment of skin pigmentation in sunprotected and sunexposed areas of skin by reflectance spectrometry at baseline.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTcholecalciferolGiven orally
OTHERplaceboGiven orally

Timeline

Start date
2009-02-01
Primary completion
2012-06-01
Completion
2012-06-01
First posted
2009-03-27
Last updated
2013-09-16

Locations

2 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT00870961. Inclusion in this directory is not an endorsement.