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| Sponsor: | University of California, Los Angeles |
|---|---|
| Collaborator: |
National Cancer Institute (NCI) |
| Information provided by: | University of California, Los Angeles |
| ClinicalTrials.gov Identifier: | NCT00798876 |
Purpose
Studies on patterns of how many men get prostate cancer in other countries show that environment contributes to the high incidence of prostate cancer in the United States. Epidemiology studies suggest that this influence may be reduced by the diet of men at risk of getting prostate cancer. Although the exact nature of the effects of diet are not completely known, the amount of fat eaten appears to affect the number of men who get prostate cancer. The type of fat also seems to matter. Eating more of a type of fat called omega-3 polyunsaturated fat is associated with decreased prostate cancer risk. Omega-3 fat comes from fish and is quite different from the type of fat from animals and vegetables (omega-6 fat). Because the exact mechanism of this reduction in prostate cancer risk is not known, no blood test indications, called markers, have been discovered that would show the effect working.
Study doctors designed this study to try to find markers in the blood tests of men who have prostate cancer, and to find out if a diet supplemented with omega-3 type fat from fish oil helps reduce those markers, hence indicating that it helps reduce the cancer in these men. These men will be compared to men with prostate cancer whose diets do not contain the fish-oil fat.
The men chosen will have prostate cancer and be scheduled for operations to have their prostate glands removed. They will be chosen randomly to be given the fish-oil diet or a regular Western diet for comparison for 4 to 8 weeks. Their blood will be checked at the beginning of the diet. After the 4-to-8-week period, they will have their operations. Their blood will be checked again and a sample of their removed prostate will be examined to tell if the diet had any effect on the cancer and its markers.
| Condition | Intervention |
|---|---|
|
Prostate Cancer |
Dietary Supplement: Fish Oil Dietary Supplement: Vitamin E supplement Dietary Supplement: Western Diet Dietary Supplement: Low-Fat Diet Other: Medical Examination Other: Dietary Interview Other: Blood Draw Procedure: Radical Prostatectomy |
| Study Type: | Interventional |
| Study Design: | Diagnostic, Randomized, Open Label, Placebo Control, Parallel Assignment, Pharmacokinetics/Dynamics Study |
| Official Title: | Comparison Study of a Low-Fat Diet Supplemented With Fish Oil and a Standard Western Diet in Individuals With Prostate Cancer |
| Estimated Enrollment: | 70 |
| Study Start Date: | August 2005 |
| Estimated Study Completion Date: | August 2009 |
| Estimated Primary Completion Date: | August 2009 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Standard Western Diet: Placebo Comparator
Subjects will be asked to consume a standard Western Diet for 4 weeks. For the 4-week period, subjects will be provided with all food and beverages. Subjects will also undergo a medical examination, dietary interview, blood draw, and radical prostatectomy(as part of standard of care).
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Dietary Supplement: Western Diet
Subjects will be provided with a standard western diet, food and beverages, to consume during their 4 week participation in this study.
Other: Medical Examination
Subjects will have a routine medical exam.
Other: Dietary Interview
Subjects will meet with the study nutritionist and have their current diet evaluated. Subjects will also undergo a test (bioimpedance) to estimate their body fat, lean weight, and the rate at which their body burns fat.
Other: Blood Draw
40 mL of blood will be drawn from subjects to measure PSA, fatty acids, insulin and various hormones.
Procedure: Radical Prostatectomy
Subjects will undergo a radical prostatectomy as part of their standard of care.
|
|
Low-Fat Diet: Experimental
Subjects will be asked to consume a low fat diet with fish oil and vitamin E supplements for 4 weeks. For the 4-week period, subjects will be provided with all food and beverages. Subjects will also undergo a medical examination, dietary interview, blood draw, and radical prostatectomy(as part of standard of care).
|
Dietary Supplement: Fish Oil
Subjects will be asked to take 10 grams of fish oil per day for 4 weeks.
Dietary Supplement: Vitamin E supplement
Subjects will be asked to take 800 International Units per day of Vitamin E for 4 weeks.
Dietary Supplement: Low-Fat Diet
Subjects will be provided with a low-fat diet (food and beverages) for their 4 week participation in this study.
Other: Medical Examination
Subjects will have a routine medical exam.
Other: Dietary Interview
Subjects will meet with the study nutritionist and have their current diet evaluated. Subjects will also undergo a test (bioimpedance) to estimate their body fat, lean weight, and the rate at which their body burns fat.
Other: Blood Draw
40 mL of blood will be drawn from subjects to measure PSA, fatty acids, insulin and various hormones.
Procedure: Radical Prostatectomy
Subjects will undergo a radical prostatectomy as part of their standard of care.
|
Eligibility| Ages Eligible for Study: | 40 Years to 75 Years |
| Genders Eligible for Study: | Male |
| Accepts Healthy Volunteers: | No |
Eligibility Criteria:
Contacts and Locations| Contact: William Aronson, M.D. | 310-268-3446 | waronson@ucla.edu |
| United States, California | |
| UCLA Jonsson Comprehensive Cancer Center | Recruiting |
| Los Angeles, California, United States, 90095 | |
| Contact: William Aronson, MD 310-268-3446 waronson@ucla.edu | |
| Sub-Investigator: John Glaspy, MD | |
| Sub-Investigator: Pinchas Cohen, MD | |
| West Los Angeles VA | Recruiting |
| Los Angeles, California, United States, 90073 | |
| Contact: William Aronson, MD 310-268-3446 waronson@ucla.edu | |
| Principal Investigator: | William Aronson, MD | UCLA and Western Los Angles VA |
More Information
| Responsible Party: | UCLA ( William Aronson, MD ) |
| Study ID Numbers: | 01-07-026, P50 CA 92131-01A1 |
| Study First Received: | November 25, 2008 |
| Last Updated: | December 2, 2008 |
| ClinicalTrials.gov Identifier: | NCT00798876 History of Changes |
| Health Authority: | United States: Institutional Review Board |
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Antioxidants Genital Neoplasms, Male Prostatic Diseases Molecular Mechanisms of Pharmacological Action Growth Substances Physiological Effects of Drugs Urogenital Neoplasms Genital Diseases, Male |
Protective Agents Pharmacologic Actions Neoplasms Vitamin E Neoplasms by Site Vitamins Micronutrients Prostatic Neoplasms |