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Brassica Vegetables or Indole-3-Carbinol in Treating Patients With PSA Recurrence After Surgery for Prostate Cancer

Primary Purpose

Prostate Cancer

Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
behavioral dietary intervention
Brassica vegetable
indole-3-carbinol
counseling intervention
medical chart review
questionnaire administration
adjuvant therapy
Sponsored by
Vanderbilt University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Prostate Cancer focused on measuring recurrent prostate cancer

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)MaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Diagnosis of prostate cancer with PSA recurrence after prostatectomy

    • PSA recurrence is defined as two consecutively rising PSA tests ≥ 8 weeks since the post-surgical nadir, with a minimal interval of 2 weeks between tests and at least 1 PSA test > 0.4 ng/mL

Exclusion Criteria:

  • Life expectancy ≥ 9 months
  • No predictors of poor adherence (e.g., erratic life-style, mental incompetence)

PRIOR CONCURRENT THERAPY:

  • See Disease Characteristics
  • No other concurrent Brassica vegetable consumption > 1 serving/day
  • No other concurrent indole-3-carbinol supplements
  • No endocrine or radiation treatment within past 4 weeks
  • No other scheduled treatment during study intervention
  • Concurrent prescription medications during the trial allowed

    • At least 2 weeks since prior and no concurrent vitamin or herbal supplement use

      • Patients refusing to stop non-study supplements will be asked to maintain constant use

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    Experimental

    Arm Label

    Brassica Vegetables Diet Intervention

    Pill

    Arm Description

    Outcomes

    Primary Outcome Measures

    Feasibility of Brassica vegetable intake and indole-3-carbinol supplementation
    Adverse events
    Effects of intervention on prostate-specific antigen

    Secondary Outcome Measures

    Full Information

    First Posted
    February 1, 2008
    Last Updated
    April 26, 2016
    Sponsor
    Vanderbilt University
    Collaborators
    National Cancer Institute (NCI)
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    1. Study Identification

    Unique Protocol Identification Number
    NCT00607932
    Brief Title
    Brassica Vegetables or Indole-3-Carbinol in Treating Patients With PSA Recurrence After Surgery for Prostate Cancer
    Official Title
    Effects of Bassica or Indole-3-Carbinol on Prostatectomy Patients With PSA Recurrence
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    April 2016
    Overall Recruitment Status
    Completed
    Study Start Date
    March 2005 (undefined)
    Primary Completion Date
    January 2007 (Actual)
    Study Completion Date
    November 2010 (Actual)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Vanderbilt University
    Collaborators
    National Cancer Institute (NCI)

    4. Oversight

    Data Monitoring Committee
    Yes

    5. Study Description

    Brief Summary
    RATIONALE: Eating a diet high in vegetables may lower the risk of some types of cancer. Brassica vegetables (such as cabbages, kale, broccoli, Brussels sprouts, and cauliflower) and indole-3-carbinol (a substance found in cruciferous vegetables) may help lower the risk of prostate cancer recurrence. PURPOSE: This randomized clinical trial is studying the side effects and how well Brassica vegetables work compared with indole-3-carbinol in treating patients with PSA recurrence after surgery for prostate cancer.
    Detailed Description
    OBJECTIVES: Determine the feasibility of Brassica vegetable intake and indole-3-carbinol supplement use in patients with prostate cancer with prostate-specific antigen (PSA) recurrence after prostatectomy. Identify adverse events in these patients. Quantify the effects of each intervention on PSA in these patients. OUTLINE: Patients are stratified by pretreatment prostat-specific antigen (PSA) growth rate (low [0.00-0.15] vs medium [0.16-0.30] vs high [> 0.30]). They are randomized to 1 of 3 treatment arms, and randomization status to arms II and III is double-blinded. Arm I (Brassica vegetables): Patients consume Brassica vegetables at least 2 servings (½ cup/serving) daily for 6 months. Patients meet one-on-one with the study dietician, and are instructed on the potential health benefits of Brassica vegetables and purchase and preparation of the vegetables. Patients undergo telephone counseling periodically in months 1-5, to monitor their progress and identify barriers to adherence and to develop solutions to overcome these barriers. Arm II (Placebo): Patients receive oral placebo once daily for 6 months. Arm III (Indole-3-carbinol supplement): Patients receive oral indole-3-carbinol supplement (capsules) once daily for 6 months. Blood and urine samples (for urinary isothiocyanate levels) are collected at baseline and at 2, 4, and 6 months. Patients complete questionnaires assessing demographics, family cancer history, and health history and measuring changes in medications, lifestyle, adverse events, and health. Medical records are reviewed for prostate cancer-related information, surgical dates, dose and type of radiation, and PSA history.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Prostate Cancer
    Keywords
    recurrent prostate cancer

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Masking
    ParticipantInvestigator
    Allocation
    Randomized
    Enrollment
    66 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    Brassica Vegetables Diet Intervention
    Arm Type
    Experimental
    Arm Title
    Pill
    Arm Type
    Experimental
    Intervention Type
    Behavioral
    Intervention Name(s)
    behavioral dietary intervention
    Intervention Type
    Dietary Supplement
    Intervention Name(s)
    Brassica vegetable
    Intervention Type
    Drug
    Intervention Name(s)
    indole-3-carbinol
    Other Intervention Name(s)
    I3C
    Intervention Description
    follow up at 2,4,6 months post baseline.
    Intervention Type
    Other
    Intervention Name(s)
    counseling intervention
    Intervention Description
    2, 4, 6 months post baseline
    Intervention Type
    Other
    Intervention Name(s)
    medical chart review
    Intervention Description
    2,4,6 months post baseline
    Intervention Type
    Other
    Intervention Name(s)
    questionnaire administration
    Intervention Type
    Procedure
    Intervention Name(s)
    adjuvant therapy
    Primary Outcome Measure Information:
    Title
    Feasibility of Brassica vegetable intake and indole-3-carbinol supplementation
    Time Frame
    will be measured at 2-Months, 4-Months, and 6-Months after Baseline start for the diet intervention
    Title
    Adverse events
    Time Frame
    will be measured at 2-Months, 4-Months, and 6-Months after Baseline start for the diet intervention
    Title
    Effects of intervention on prostate-specific antigen
    Time Frame
    Not noted

    10. Eligibility

    Sex
    Male
    Minimum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Diagnosis of prostate cancer with PSA recurrence after prostatectomy PSA recurrence is defined as two consecutively rising PSA tests ≥ 8 weeks since the post-surgical nadir, with a minimal interval of 2 weeks between tests and at least 1 PSA test > 0.4 ng/mL Exclusion Criteria: Life expectancy ≥ 9 months No predictors of poor adherence (e.g., erratic life-style, mental incompetence) PRIOR CONCURRENT THERAPY: See Disease Characteristics No other concurrent Brassica vegetable consumption > 1 serving/day No other concurrent indole-3-carbinol supplements No endocrine or radiation treatment within past 4 weeks No other scheduled treatment during study intervention Concurrent prescription medications during the trial allowed At least 2 weeks since prior and no concurrent vitamin or herbal supplement use Patients refusing to stop non-study supplements will be asked to maintain constant use
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Jay H. Fowke, PhD, MPH
    Organizational Affiliation
    Vanderbilt-Ingram Cancer Center
    Official's Role
    Study Chair

    12. IPD Sharing Statement

    Learn more about this trial

    Brassica Vegetables or Indole-3-Carbinol in Treating Patients With PSA Recurrence After Surgery for Prostate Cancer

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