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Completed

NCT Number: NCT00706121

S0000D: Effect of Vitamin E and/or Selenium on Colorectal Polyps in Men Enrolled on SELECT Trial SWOG-S0000

RATIONALE: Studying tissue samples in the laboratory from participants receiving treatment on the Selenium and Vitamin E Cancer Prevention Trial (SELECT) SWOG-S0000 may help doctors predict a participant's response to treatment and help plan the best treatment.

PURPOSE: This phase III trial is studying the effect of vitamin E and/or selenium on colorectal polyps in men enrolled on SELECT Trial SWOG-S0000.

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Key information

About this study

OBJECTIVES:

Primary

  • To assess the effect of selenium on colorectal adenoma (CRA) occurrence.
  • To assess the effect of selenium on number, location, size, histologic type, and degree of dysplasia of CRA.
  • To assess the effect of selenium on colorectal cancer (CRC) incidence.

Secondary

  • To assess the effect of vitamin E on CRA occurrence.
  • To assess the effect of vitamin E on CRC incidence.

Tertiary

  • To explore the effect modification of selenium and vitamin E by aspirin on CRA occurrence.
  • To explore the effect modification of selenium and vitamin E by body mass index.

OUTLINE: This is a multicenter study.

Endoscopically obtained tissue samples are reviewed by study pathologists to confirm the presence (or absence) of a colorectal adenoma (CRA). If a CRA is present, the number, location, size, histology, and degree of dysplasia are documented. The CRA is also reviewed to exclude a diagnosis of colorectal cancer.

Additional data, including aspirin use, height and weight, date of birth, and other demographic and baseline characteristics, is also obtained. Participants' medical records are reviewed periodically.

Participants are followed annually.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

DISEASE CHARACTERISTICS:

  • Enrolled on the Selenium and Vitamin E Cancer Prevention Trial (SELECT) SWOG-S0000
  • Screened by lower endoscopy (i.e., sigmoidoscopy and/or colonoscopy) after randomization on SELECT trial

PATIENT CHARACTERISTICS:

  • Willing to sign an applicable medical records release form
  • Willing to allow the release of tissue for central pathology review of resected polyps and endoscopic biopsies

PRIOR CONCURRENT THERAPY:

  • See Disease Characteristics

Treatment and study plan

Vitamin E

Drug

400 IU daily by mouth for 7 - 12 years

Other names: alpha tocopherol

selenium

Drug

200 mcg daily for 7 - 12 years

Other names: L-selenomethionine

vitamin E placebo

Drug

1 pill by mouth daily for 7 - 12 years

Other names: placebo

selenium placebo

Drug

1 pill by mouth daily for 7 - 12 years

Other names: placebo

Primary outcomes

  1. Effect of Selenium on Colorectal Adenoma (CRA) Occurrence, Analyzed by Active Selenium vs. Selenium Placebo

    Time frame: From 1 year post randomization through study completion

  2. Effect of Selenium on Advanced Neoplasia, Analyzed by Active Selenium vs. Selenium Placebo

    Time frame: From 1 year post randomization through study completion

    Adenomas with diameter >=1cm or any adenoma with villous features or high-grade dysplasia

  3. Effect of Selenium and/or Vitamin E on Colorectal Cancer (CRC) Incidence

    Time frame: From 1 year post randomization through study completion

  4. Effect of Selenium on Occurrences of Multiple (>2) Adenomas

    Time frame: From 1 year post randomization through study completion

Secondary outcomes

  1. Effect of Vitamin E on CRA Occurrence, Analyzed by Active Vitamin E vs. Vitamin E Placebo

    Time frame: From 1 year post randomization through study completion

Other outcomes

  1. Effect Modification of Selenium by Body Mass Index on CRA Occurrence, Analyzed by Active Selenium vs. Selenium Placebo

    Time frame: From 1 year post randomization through study completion

  2. Effect Modification of Selenium by Aspirin on CRA Occurrence, Analyzed by Active Selenium vs. Selenium Placebo

    Time frame: From 1 year post randomization through study completion

  3. Effect Modification of Vitamin E by Body Mass Index on CRA Occurence, Analyzed by Active Vitamin e vs. Vitamin e Placebo

    Time frame: From 1 year post randomization through study completion

  4. Effect Modification of Vitamin E by Aspirin on CRA Occurrence, Analyzed by Active Vitamin e vs. Vitamin e Placebo

    Time frame: From 1 year post randomization through study completion

Sponsors and collaborators

Lead sponsor

SWOG Cancer Research Network

Network

Collaborators

  • National Cancer Institute (NCI)

Registry information

Official study title

S0000D: A Study of the Effect of Vitamin E and/or Selenium on Adenomatous Colorectal Polyps (ACP) in Participants Enrolled in SELECT

Acronym: ACP

Important dates

Study start
2008
Primary completion
2015
Study completion
2018
First posted
Jun 27, 2008
Registry last updated
Dec 16, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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