Efficacy and Toxicity of Bicalutamide and Dutasteride vs. Standard Care for Prostate Cytoreduction for Brachytherapy

PHASE2CompletedINTERVENTIONAL
Enrollment

60

Participants

Timeline

Start Date

March 31, 2009

Primary Completion Date

March 31, 2019

Study Completion Date

December 31, 2019

Conditions
Prostate CancerErectile DysfunctionLower Urinary Tract Symptoms
Interventions
DRUG

administration of a LHRH agonist and Bicalutamide

3-month treatment with an LHRH agonist chosen by the treating radiation oncologist and Bicalutamide 50 mg daily for the first month of treatment with the LHRH agonist.

DRUG

administration of Bicalutamide, Dutasteride and Tamoxifen

"Dutasteride given at dose of 0.5 mg daily starting three months prior to day of implant procedure and continued for 3 months up until procedure.~Bicalutamide: given at a dose of 50 mg daily for 3 the same 3 month period as dutasteride~Tamoxifen: given at dose of 10 mg daily for 3 months that dutasteride and bicalutamide are administered."

Trial Locations (1)

G1R 2J6

CHUQ- Hotel-Dieu de Quebec, Québec

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

GlaxoSmithKline

INDUSTRY

lead

CHU de Quebec-Universite Laval

OTHER

NCT00866554 - Efficacy and Toxicity of Bicalutamide and Dutasteride vs. Standard Care for Prostate Cytoreduction for Brachytherapy | Biotech Hunter | Biotech Hunter