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Active, not recruitingNCT01653925Updated Nov 24, 2025

Molecular Mechanisms of Dutasteride and Dietary Interventions to Prevent Prostate Cancer and Reduce Its Progression

An interventional study of Dietary intervention first and Drug (Dutasteride) intervention first in Prostatic Neoplasms and Low Grade Prostate Cancer, sponsored by CHU de Quebec-Universite Laval. Active, not recruiting at 2 sites in Canada. Open to male participants aged 35 Years to 75 Years. Per ClinicalTrials.gov, last updated 2025-11-24.

Sponsored by CHU de Quebec-Universite Laval · Not applicable, Interventional, and Prevention

From the registry’s dates

  • Registered 1 year 8 months after the study started (first participant enrolled Oct 2010, registered Jul 2012).
Phase
Not applicable
Study type
Interventional
Enrollment
120
Allocation
Randomized
Ages
35 Years to 75 Years
Sex
Male
01

Study summary

The purpose of this study is to determine whether marine omega-3 fatty acids and 5-alpha-reductase inhibitor are effective in the progression of prostate cancer for low-risk prostate cancer patients.

Read the detailed description

The study has a duration of 1 year for each participant. Subjects will be first assigned to a dietary or a dutasteride intervention that they will consume for the first 6 months. After 6 months, all men will have a combined intervention of dutasteride and diet to complete follow-up of 12 months. This will allow us to study interactive effects.

Dietary intervention consists on a high w-3 long-chain fatty acids diet without supplement and to reduce intake of saturated and trans fatty acids.

Prostatic biopsies will be taken at time of diagnosis and at 6 and 12 months after the beginning of the study. Blood will be drawn before each prostate biopsy session and urine will be collected before each prostate biopsy and after digital rectal examination.

02

Conditions studied

  • Prostatic Neoplasms
  • Low Grade Prostate Cancer

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Keywords

  • Prostatic Neoplasms
  • Low grade prostate cancer
03

In context

Prostatic Neoplasms

6,370 studies on the registry are indexed under Prostatic Neoplasms; 1,400 are open to participants now.

This study's enrollment of 120 is above the median of 58 across 4,822 interventional studies indexed under Prostatic Neoplasms.

Browse Prostatic Neoplasms studies →

Lead sponsor

CHU de Quebec-Universite Laval is the lead sponsor of 134 studies on the registry; 27 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
35 Years to 75 Years
Sexes eligible
Male
Accepts healthy volunteers
No

Inclusion criteria

  • Low-risk prostatic neoplasms
  • Candidate for active surveillance
  • Informed consent

Exclusion criteria

Exclusion Criteria:

  • Current fish oil supplementation
  • Current NSAID use
05

Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Factorial assignment
Masking
None (open label)
Enrollment
120 participants (actual)

Study arms

  • Experimental
    Dietary intervention first

    The dietary intervention will be aimed to increase intake of ω-3 long chain fatty acids and to reduce intake of saturated and trans fatty acids.

    Other: Dietary intervention first

  • Experimental
    Drug intervention first

    Intake of 5α-Reductase Inhibitor

    Drug: Drug (Dutasteride) intervention first

Interventions

  • OtherDietary intervention first

    The dietary intervention will be aimed to increase intake of ω-3 long chain fatty acids and to reduce intake of saturated and trans fatty acids. Three consultations with a nutritionist experienced in clinical trials will be planned over a 6-month period. An additional 2 consultations in the last 6 months with the study nutritionist will be planned for men allocated to the dietary fat intervention arm first. Then, after the 6 months of diet intervention, drug intervention with 5α-Reductase Inhibitor will be add to diet for the 6 following months.

    Also known as: Dutasteride

  • DrugDrug (Dutasteride) intervention first

    5α-Reductase Inhibitor will be taken daily in tablet dosage form (0.5 mg) taken orally for 12 months depend of the group. After 6 months of drug intake, dietary fat intervention will be add to treatment for the following 6 months. Three consultations with a nutritionist experienced in clinical trials will be planned over this 6-month period.

    Also known as: Dutasteride

06

What researchers measure

Primary outcomes

  1. Effects of the Interventions on Lipid Metabolism From Blood and Prostatic Microenvironment

    In this aim the investigators will measure the effects of the interventions on the fatty acid profile of phospholipids from RBC and from snap frozen prostate tissue. Fatty acid profile from prostatic tissue has never been studied. The investigators aim that change in fatty acid intake will affect fatty acid profile of prostatic tissue. Fatty acid profile from red blood cells will serve as a marker of dietary fatty acid intake. Previous studies have shown that fatty acids profile from RBC differs from the one from muscle tissue and that the dietary effect on RBC fatty acids profile is almost maximal within 6 months.

    Time frame: 0-6-12 months

Secondary outcomes

  1. Effect of Interventions on Gene Expression Profile

    In this aim the investigators will investigate how the interventions affect prostate tissue gene expression profile determined by cDNA micro-array analysis. We hypothesize that a down-regulation will occur in genes associated with inflammation, androgen synthesis, cell proliferation and angiogenesis pathways. Also, this prospective study provides an opportunity of a retrospective comparison of baseline gene expression patterns from initial prostate biopsy will be correlated with baseline self-reported dietary intake.

    Time frame: 0-6-12 months

  2. Effects of Interventions on Hormonal Metabolism

    The investigators will initially focus our attention on estrogens (Estrone, Estradiol) and most important androgens and their metabolites (dihydrotestosterone, testosterone, 3-α-diolglucuronide, androsterone glucuronide).

    Time frame: 0-6-12 months

  3. Determine the Clinical Utility of Urine-Based Cancer Markers in the Context of Interventions to Reduce Cancer Progression

    Although one of the best tumor markers available to monitor disease recurrence after treatment, PSA lacks specificity to monitor patients on active surveillance. The expression of urinary PCA3 (developed in Québec) improves the diagnosis of prostate cancer over standard parameters, including PSA, and the PCA3 score was shown to correlate with grade, stage and tumor volume in prostatectomy specimen. Another gene-based marker, the TMPRSS2-ERG gene fusion transcript, is also associated with tumor aggressiveness and detected in urine.

    Time frame: 0-6-12 months

07

Study locations

2 sites
  • Hotel-Dieu of Quebec
    Québec, Quebec G1R 2J6, Canada
  • Institute of nutraceuticals and functional food of Laval University
    Québec, Quebec G1V 0A6, Canada
08

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Nov 24, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT01653925
Lead sponsor
CHU de Quebec-Universite Laval
Collaborators
Prostate Cancer Canada
Responsible party
Sponsor
First posted
Jul 31, 2012
Start date
Oct 28, 2010
Primary completion
Dec 31, 2016
Completion
Dec 2026 (estimated)
Last update
Nov 24, 2025

Study contacts

Vincent Fradet, MD
principal investigator · Laval University

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is active, not recruiting, as verified in Nov 2025. You cannot join it, but the record below documents what was studied.

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