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Clinical Trials in Canada / NCT02333435
Active, not recruiting Phase 2

Effects of EPA on Prostate Cancer Cells Proliferation and Quality of Life

NCT02333435 · tracked via the Priya Life Science Canada tracker
Phase
Phase 2
Started
2015-02-12
Last updated
2025-11-20

Condition(s) studied

Prostate Cancer

Investigational drug(s) / intervention(s)

EPAPlacebo

EPA: 3g/day of purified EPA , capsules, taken once daily, for 14 months

Placebo: 3g/day of placebo (high oleic sunflower oil) , capsules, taken once daily, for 14 months

Study summary

Prostate cancer, the most frequently diagnosed cancer among occidental men, is associated with a major individual and societal burden. Although still controversial, the literature suggests that a high consumption of omega-3 fatty acids (ω3) has protective effects against prostate cancer. One of the proposed mechanisms of action of ω3 lies in their anti-inflammatory properties. In addition, there are some observational evidences suggesting an association of ω3 intake with a lower rate of depression in cancer patients. However, no clinical study has tested the efficacy of ω3 supplementation on psychological and quality of life outcomes in that population. Several evidences point to a possible involvement of inflammation in psychological issues. Reducing the systemic inflammatory state may have beneficial impact on the quality of life of these patients. Preliminary work from this team of investigators, in a cohort of patients managed with active surveillance for their low-grade prostate cancer, show a strong inverse association between the risk of prostate cancer progression (to high-grade) and the level of prostatic eicosapentanoic acid (EPA- a type of ω3).

HYPOTHESIS: EPA-rich monoglycerides fish oil (MAG-EPA) has global positive effects on prostate cancer cell proliferation, inflammation and on the patient's psychosocial functioning and quality of life.

The investigators propose a double blind, randomized controlled clinical trial. 130 consecutive patients suffering from high-risk prostate cancer who choose to be treated by radical prostatectomy will be eligible to this study. The presence of high-grade cancer will be mandatory.

The intervention, a daily supplementation with 3g supplement of fish oil monoglycerides rich in EPA, vs. placebo capsules containing high oleic sunflower oil, will start six weeks before the prostatectomy and will continue for one year after surgery. The potential confounding variables will be measured before the start of the intervention: age, anthropometric parameters, stage and clinical and pathological tumor grade (Gleason score), pre-operative level of prostate specific antigen and diet.

This project proposes a simple intervention by dietary supplementation that could eventually help to reduce the incidence and/or progression of prostate cancer, and the consequences of its treatment, and thus could contribute to diminish the heavy individual and societal burden of prostate cancer. The clinical data generated by this trial will serve as solid basis for a large-scale phase III clinical trial.

Eligibility

Sex
MALE
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Prostate cancer (Gleason score \>= 7) * Patient has chosen to undergo radical prostatectomy * Patient agrees to stop taking any omega-3 supplements at least 3 months before the start of the study * Patient has provided informed consent Exclusion Criteria: * Allergy to fish and sunflower * Suffering from a bipolar disorder

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Centre de Recherche Clinique et Evaluative en Oncologie - Hotel Dieu de Quebec Québec Quebec

More CHU de Quebec-Universite Laval trials in Canada

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT02333435 on ClinicalTrials.gov ↗ ← All trials in Canada