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Lucrin® Depot Efficacy and Safety Monitoring Study in Patients With Advanced Prostate Cancer and Lower Urinary Tract Symptoms (LUTS)

2014-08-27 03:15:31 | BioPortfolio

Summary

The purpose of the study is to determine the influence of luteinizing hormone releasing hormone (LHRH) analogue - Lucrin Depot 11,25 mg (Lucrin Depot 3,75mg - in Ukraine) administration on intensity of lower urinary tract symptoms (LUTS) in patients with diagnosed locally advanced and/or metastatic prostatic cancer and LUTS.

Description

The remaining targets are:

- to assess the intensity of LUTS in population of polish patients with locally advanced and/or metastatic prostatic cancer, previously untreated with hormonal therapy,

- to assess the prevalence of other symptoms in population of polish patients with locally advanced and/or metastatic prostatic cancer (such as: hematospermia, epigastric pain, urine incontinence, erection disturbances, crotch pain, anal pain or bleeding, lumbar/back pain, bones pain, spinal compression symptoms, peripheral lymph nodes enlargement, lymphatic oedema of lower extremities),

- to assess the influence of LHRH analogue (Lucrin Depot 11,25 mg in Poland, Lucrin Depot 3,75mg in Ukraine) administration on intensity of other symptoms in patients with prostatic cancer,

- to provide data on safety of Lucrin Depot treatment during 15-month therapy course

Study Design

Observational Model: Case-Only, Time Perspective: Prospective

Conditions

Advanced Prostate Cancer

Intervention

Leuprolide acetate Depot Susp. 11,25 mg (Poland), 3,75 mg (Ukraine)

Location

Site Reference ID/Investigator# 31076
Belchatow
Poland
97-400

Status

Active, not recruiting

Source

Abbott

Results (where available)

View Results

Links

Published on BioPortfolio: 2014-08-27T03:15:31-0400

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