Effects Of Dutasteride On Risk Reduction Of Acute Urinary Retention Relapse Following Trial Without Catheter

GlaxoSmithKline (GSK)

Status and phase

Terminated

Phase 4

Conditions

Benign Prostatic Hyperplasia

Treatments

Drug: Dutasteride

Study type

Interventional

Funder types

Industry

Identifiers

NCT00421421

ARI106807

Details and patient eligibility

About

The purpose of this study is to evaluate the efficacy and safety of dutasteride at reducing relapse rates of Acute Urinary Retention (AUR), including reduction in surgical intervention for benign prostatic hyperplasia (BPH), in patients who receive a 6 month treatment of dutasteride (0.5mg once daily) following a single episode of AUR followed by successful Trial Without Catheter compared with placebo.

Sex

Male

Ages

50+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Able to read, write and understand instructions related to study procedures and able to give written informed consent
Able to swallow and retain oral medication
Had a single, spontaneous episode of AUR related to BPH with a drained volume of between 500 and 1500ml
Had a successful TWOC (defined as successful if the patient returns to satisfactory voiding within the first 24 hours after catheter removal without re-catheterisation) following 2 - 3 days treatment with alpha blocker (preferably alfuzosin 10mg OD) pre TWOC followed by up to seven days treatment with alpha blocker (preferably alfuzosin 10mg OD) post TWOC.
Able to be randomised within 7 days of successful TWOC

Exclusion criteria

Prostate volume (PV) of less than 30cc and greater than 80cc measured via Trans Rectal Ultrasound (TRUS) either at time of hospitalisation or as part of the screening / randomisation visit
Previous episode of AUR prior to the current episode
AUR not related to BPH i.e. postoperative retention following major abdominal / pelvis surgery
Previous prostate or urethral surgery
Previous positive prostate biopsy
Any cause other than BPH that may result in urinary symptoms or changes in flow rates.
Any unstable co-existing medical condition
Previous 5-ARI use
Previous alpha blocker treatment other than the study mandated 2 - 3 days pre and up to 7 days post TWOC period with alpha blocker (preferably alfuzosin 10mg OD)
Use of prohibited meds (e.g. 5ARI's, anabolic steroids including testosterone, drugs with antiandrogenic properties)
Liver enzymes (ALT, AST, ALP) at time of hospitalisation / screening visit greater than 2 x ULN or bilirubin at time of hospitalisation / screening visit greater than 1.5 x ULN.
Serum creatinine at time of hospitalisation / screening visit greater than 1.5 x ULN
Treatment with any other investigational product within 30 days prior to the first dose of study medication
History or current evidence of alcohol or drug abuse within the last 12 months
Prostate Specific Antigen (PSA) greater than 20ng/ml
Use of suprapubic catheterisation after failed urethral catheterisation
Neurogenic bladder dysfunction, confirmed or suspected, irrespective of etiology
Isolated bladder neck disease
Acute or chronic prostatitis
Confirmed or suspected urethral stricture
Known bladder stones
Clot retention secondary to haematuria of any cause
Patient unwilling to use a condom during sexual intercourse