Randomized Trial Comparing Alfuzosin GITS 10 mg Daily With Placebo for Trial Without Catheter in Acute Urinary Retention With Long Term Follow up
NCT00563654 · Status: TERMINATED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 48
Last updated 2011-06-16
Summary
The purpose of the study is to compare alfuzosin GITS once daily versus placebo in achieving a successful TWOC after AUR due to BPH, among Chinese males in Hong Kong, and in delaying or avoiding a TURP.
Conditions
- Prostatic Hyperplasia
- Urinary Retention
- Acute Disease
Interventions
- DRUG
-
Alfuzosin GITS (Xatral XL)
Sponsors & Collaborators
-
Hospital Authority, Hong Kong
lead OTHER_GOV
Principal Investigators
-
Chi Wai Cheng, Dr · Department of Surgery, Division of Urology, North District Hospital
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 50 Years
- Sex
- MALE
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2005-10-31
- Completion
- 2006-11-30
Countries
- China
Study Locations
More Related Trials
-
Evaluation of Symptom-specific Goal Achievement
NCT00836823 ·Status: COMPLETED ·Phase: PHASE4
-
Clinical Trial in Males With BPH (Enlarged Prostate)
NCT00029822 ·Status: COMPLETED ·Phase: PHASE3
-
ALFAURUS : A DB Randomized Parallel Group Study of Alfuzosin 10mg OD vs Placebo in the Management of AUR in Patients With a 1st Episode Due to BPH
NCT00290030 ·Status: COMPLETED ·Phase: PHASE3
-
Sexuality And Management of Benign Prostatic Hyperplasia With Alfuzosin
NCT00401661 ·Status: COMPLETED ·Phase: PHASE4
-
Efficacy and Safety of Alfuzosin for the Treatment of Voiding Dysfunction in Female
NCT00679315 ·Status: COMPLETED ·Phase: PHASE2
-
Alfuzosin XL Lower Urinary Tract Symptoms Efficacy and Sexuality Study
NCT00575913 ·Status: COMPLETED ·Phase: PHASE4
-
Efficacy and Safety of SL77.0499-10 (Alfuzosin) Versus Placebo and Tamsulosin in Japanese Patients With Benign Prostatic Hyperplasia
NCT00399464 ·Status: COMPLETED ·Phase: PHASE3
-
ALF-ONE : ALFuzosin ONcE Daily
NCT00280605 ·Status: COMPLETED ·Phase: PHASE4
-
Long Term Safety of SL77.0499-10 (Alfuzosin) in Patients With BPH
NCT00347061 ·Status: COMPLETED ·Phase: PHASE3
-
Benign Prostatic Hyperplasia in Taiwan
NCT00941343 ·Status: COMPLETED ·Phase: NA
-
The Efficacy, Onset of Effect, and Safety of Alfuzosin Once Daily in the Treatment of Lower Urinary Tract Symptoms of Benign Prostatic Hyperplasia: A Randomized, Placebo-Controlled Trial Using an Acute International Prostate Score
NCT00540891 ·Status: COMPLETED ·Phase: PHASE3
-
Efficacy of α-blocker or 5-ARI Withdrawal to Continued Combination Therapy on the Maintenance of LUTS in Men With BPH
NCT05023824 ·Status: UNKNOWN ·Phase: PHASE3
-
Once Daily Given Alfuzosin in the Treatment of BPH
NCT00637715 ·Status: COMPLETED ·Phase: PHASE4
-
An Efficacy Study to Evaluate Alfuzosin to Treat Men With Erectile Dysfunction and Mild Lower Urinary Tract Symptoms
NCT00893113 ·Status: COMPLETED ·Phase: PHASE3
-
Antimuscarinics as the First-line Treatment for Male With IPSS-V/S≤1
NCT01661621 ·Status: COMPLETED ·Phase: PHASE4
-
(Phosphodiesterase 5 Inhibitors & α-blockers): Single Versus Combined Therapy in Benign Prostatic Hyperplasia
NCT05236634 ·Status: UNKNOWN ·Phase: NA
-
Trial to Compare Alfuzosin Versus Placebo in the Treatment of Chronic Prostatitis/Chronic Pelvic Pain Syndrome
NCT00103402 ·Status: COMPLETED ·Phase: PHASE3
-
Clinical Progression and Costs in Benign Prostatic Hyperplasia Patients Treated With Early Versus Delayed Combination Therapy
NCT01435954 ·Status: COMPLETED
-
Efficacy and Safety of a Single TRUS-guided Intraprostatic Injection of NX-1207 in Patients With LUTS Due to BPH
NCT02003742 ·Status: TERMINATED ·Phase: PHASE3
-
Advanced Benefits of Alpha-blocker Monotherapy on Lower Urinary Tracts Symptoms(LUTS) Patients
NCT01736033 ·Status: UNKNOWN ·Phase: PHASE4
-
Dose Ranging Study of Alfuzosin in Patients With Lower Urinary Tract Symptoms Related to Benign Prostatic Hyperplasia
NCT00409357 ·Status: COMPLETED ·Phase: PHASE2
-
MCS in Treating Lower Urinary Tract Symptoms (LUTS) Suggestive of Benign Prostatic Hyperplasia
NCT00501371 ·Status: TERMINATED ·Phase: PHASE3
-
A Study to Evaluate the Tolerability and Efficacy of Tamsulosin 0.4mg OCAS Formulation in Patients Who Are Unsatisfied With the Treatment of Tamsulosin 0.2mg Conventional Formulation
NCT02180789 ·Status: COMPLETED ·Phase: PHASE4
-
Uroxatral in Men With Benign Prostate Hypertrophy (BPH) and Erectile Dysfunction (ED)
NCT00256399 ·Status: COMPLETED ·Phase: NA
-
Study to Investigate the Efficacy and Safety of GL2702 GLARS-NF1tablet and Harnal-D - Tablet in BPH Patients With LUTS
NCT02303769 ·Status: COMPLETED ·Phase: PHASE3