Phase I Biomarker Study of Dietary Grape-derived Low Dose Resveratrol for Colon Cancer Prevention
NCT ID: NCT00578396
Last Updated: 2021-01-25
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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WITHDRAWN
PHASE1
INTERVENTIONAL
2007-12-31
2007-12-31
Brief Summary
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Detailed Description
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In this study, we will directly test the impact of a diet containing a specific amount of red grapes in the context of a controlled amount of other resveratrol containing foodstuffs on Wnt signaling in the colon. This grape-supplemented diet provides a low-dose of resveratrol in conjunction with other potentially active components contained within the grapes. Participants will be normal volunteers and molecular studies will be done on colon tissue obtained by a limited flexible sigmoidoscopy before, and after, the red grape-containing diet is ingested. Different dosages of grapes will be utilized. This study will define the effect of dietary grape-derived low dose resveratrol on biomarkers related to the Wnt pathway, and provide critical information as to the utility of this nutritional approach toward colon cancer prevention.
For this study, seedless red grapes will be used. Ten participants will be enrolled at each dose level of grapes as follows:
* Dose level 1: 1 lb/day fresh red grapes
* Dose level 2: 2/3 lb/day fresh red grapes
* Dose level 3: 1/3 lb/day fresh red grapes
Participants will be normal volunteers identified through advertisements, referrals, and community outreach.
Primary Objective:
Define the minimum dietarily achievable amount of resveratrol-rich fresh red grapes which are effective in inhibiting Wnt signaling in human colonic mucosa.
Secondary Objectives
1. Define whether grape-supplemented diet affects colonic mucosa cell proliferation.
2. Define any side-effects associated with the resveratrol-rich dietary program.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
PREVENTION
NONE
Study Groups
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Dose Level 1
1 lb/day fresh red grapes
grapes
1 pound of seedless red grapes
Dose Level 2
2/3 lb/day fresh red grapes
grapes
2/3 lb/day fresh red grapes
Dose Level 3
1/3 lb/day fresh red grapes
grapes
1/3 lb/day fresh red grapes
Interventions
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grapes
1 pound of seedless red grapes
grapes
2/3 lb/day fresh red grapes
grapes
1/3 lb/day fresh red grapes
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* Participants must sign informed consent for enrollment
* Participants must have values for tests included in CBC, CMPAN and UA within normal range or no greater than 1.5x ULN or less than 0.75x LLN at prestudy to proceed to registration
* Participants must have normal limited flexible sigmoidoscopic examination on Day 15 to proceed to re-registration
* To receive Day 28 limited flexible sigmoidoscopy, participants must have taken \>80% of prescribed dose of red grapes (based on food diary review)
Exclusion Criteria
* Known history of diabetes
18 Years
ALL
Yes
Sponsors
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Gateway for Cancer Research
OTHER
University of California, Irvine
OTHER
Responsible Party
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Principal Investigators
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Randall F Holcombe, M.D.
Role: PRINCIPAL_INVESTIGATOR
University of California, Irvine
Locations
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University of California, Irvine Medical Center
Orange, California, United States
Countries
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Other Identifiers
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OCRT07046
Identifier Type: -
Identifier Source: org_study_id
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