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Trials / Active Not Recruiting

Active Not RecruitingNCT01653925

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

Status
Active Not Recruiting
Phase
N/A
Study type
Interventional
Enrollment
120 (actual)
Sponsor
CHU de Quebec-Universite Laval · Academic / Other
Sex
Male
Age
35 Years – 75 Years
Healthy volunteers
Not accepted

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.

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.

Conditions

Interventions

TypeNameDescription
OTHERDietary intervention firstThe 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.
DRUGDrug (Dutasteride) intervention first5α-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.

Timeline

Start date
2010-10-28
Primary completion
2016-12-31
Completion
2026-12-01
First posted
2012-07-31
Last updated
2025-11-24

Locations

2 sites across 1 country: Canada

Source: ClinicalTrials.gov record NCT01653925. Inclusion in this directory is not an endorsement.