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Status:

TERMINATED

Selenium for Prevention of Adenomatous Colorectal Polyps

Lead Sponsor:

University of Arizona

Collaborating Sponsors:

National Cancer Institute (NCI)

Conditions:

Colorectal Cancer

Adenomatous Colorectal Polyps

Eligibility:

All Genders

40-80 years

Phase:

PHASE3

Brief Summary

RATIONALE: Chemoprevention therapy is the use of certain drugs to try to prevent the development or recurrence of cancer. Selenium may be effective in preventing the recurrence of adenomatous colorect...

Detailed Description

OBJECTIVES: Primary * Compare the effects of selenium vs placebo on the recurrence of adenomatous colorectal polyps, in terms of histologic type, degree of dysplasia, number, size, and location, in ...

Eligibility Criteria

Inclusion

  • DISEASE CHARACTERISTICS:
  • Histologically confirmed colorectal adenomatous polyps
  • Meets the following criteria by colonoscopy (performed within the past 6 months):
  • Cecum was totally visualized or reached
  • At least 90% visualization of colon surface area
  • Removed at least 1 adenomatous polyp of at least 3 mm in size during procedure (For the Advanced Adenoma Sub-study: Removal of at least 1 advanced colorectal adenomatous polyp during procedure. An adenoma is considered advanced if it is 10 mm or greater in size, and/or has villous histology and/or shows high grade dysplasia)
  • Removed no more than 10 adenomatous polyps of any size by endoscopy
  • All other neoplastic and non-neoplastic colon polyps must have been completely removed (except for diminutive \[less than 3 mm\] sessile rectal polyps)
  • For the sub-study, at least 1 advanced adenomatous polyp defined as 10 mm or greater in size and/or has villous histology and/or shows high grade dysplasia
  • No prior diagnosis of any of the following:
  • Colorectal cancer
  • Familial adenomatous polyposis
  • Ulcerative colitis
  • Crohn's disease
  • Hereditary non-polyposis colon cancer (HNPCC), defined as:
  • Histologically confirmed colorectal cancer in at least 3 relatives, 1 of whom is a first-degree relative of the other 2
  • Disease occurrence in at least 2 consecutive generations
  • Colorectal cancer diagnosis in at least 1 family member who is less than 50 years of age
  • Patients with a family history of colorectal cancer but who are not diagnosed with HNPCC are allowed
  • No more than 1 prior segmental colon resection
  • PATIENT CHARACTERISTICS:
  • Age
  • 40 to 80
  • Performance status
  • SWOG 0-1
  • Life expectancy
  • Not specified
  • Hematopoietic
  • Hemoglobin \> 11 g/dL
  • WBC 3,000 - 11,000/mm\^3
  • Hepatic
  • AST and ALT \< 2 times upper limit of normal
  • Bilirubin \< 2.0 mg/dL
  • Renal
  • Creatinine \< 1.9 mg/dL
  • Cardiovascular
  • No unstable\* cardiac disease despite medication (e.g., diuretics or digitalis)
  • No uncontrolled hypertension (i.e., systolic blood pressure ≥ 170 mm Hg and/or diastolic blood pressure ≥ 110 mm Hg) despite medication NOTE: \*Unstable defined as unable to walk across the room without chest pain or shortness of breath
  • Other
  • Not pregnant or nursing
  • Fertile patients must use effective contraception for at least 2 months before and during study treatment
  • Resident of a clinical center metropolitan area or obtaining regular health care in a clinical metropolitan area for at least 6 months out of the year
  • Must be able to swallow pills
  • No unexpected weight loss of 10% or more within the past 6 months
  • No prior rheumatoid arthritis
  • No poorly controlled diabetes mellitus despite medication, defined as:
  • Blood sugar level ≥ 200 mg/dL on more than half of the readings taken within the past month
  • No invasive malignancy within the past 5 years that required medical excision, radiotherapy, or chemotherapy except basal cell or squamous cell carcinoma
  • PRIOR CONCURRENT THERAPY:
  • Biologic therapy
  • No concurrent drugs that regulate the immune system
  • Chemotherapy
  • No concurrent chemotherapy
  • Endocrine therapy
  • Not specified
  • Radiotherapy
  • No concurrent radiotherapy
  • Surgery
  • See Disease Characteristics
  • Other
  • Prior enrollment in another adenoma prevention study allowed
  • Concurrent routine aspirin (≤ 81 mg/day) allowed
  • No regular use of non-steroidal anti-inflammatory drugs (NSAIDs)
  • No concurrent enrollment in another research study using pharmacological cancer drugs, a cyclo-oxygenase-2 inhibitor, or selenium
  • No other concurrent selenium unless dosage is ≤ 50 µg/day

Exclusion

    Key Trial Info

    Start Date :

    January 20 2005

    Trial Type :

    INTERVENTIONAL

    Allocation :

    ACTUAL

    End Date :

    May 17 2018

    Estimated Enrollment :

    1621 Patients enrolled

    Trial Details

    Trial ID

    NCT00078897

    Start Date

    January 20 2005

    End Date

    May 17 2018

    Last Update

    September 24 2019

    Active Locations (7)

    Enter a location and click search to find clinical trials sorted by distance.

    Page 1 of 2 (7 locations)

    1

    Veterans Affairs Medical Center - Phoenix

    Phoenix, Arizona, United States, 85012

    2

    Virginia G. Piper Cancer Center at Scottsdale Healthcare - Shea

    Scottsdale, Arizona, United States, 85258-4512

    3

    Mayo Clinic Scottsdale

    Scottsdale, Arizona, United States, 85259-5499

    4

    Arizona Cancer Center - Tucson Clinic

    Tucson, Arizona, United States, 85724-5024