Randomized Trial Comparing Terazosin 5 mg Daily and Doxazosin GITS 4 mg Daily for Trial Without Catheter in Acute Urinary Retention With Long Term Follow up
NCT00563485 · Status: TERMINATED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 120
Last updated 2011-06-16
Summary
The purpose of the study is to compare two alpha blockers, terazosin and doxazosin GITS, 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
Interventions
- DRUG
-
Doxazosin GITS (Cardura XL)
- DRUG
-
Terazosin (Hytrin)
Sponsors & Collaborators
-
Hospital Authority, Hong Kong
lead OTHER_GOV
Principal Investigators
-
Chi Wai Cheng, Dr · Department of Surgery, Division of Urology, North District Hospital/ The Chinese University of Hong Kong
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
-
Comparison of Alpha Blockers (Terazosin and Tamsulosin) in Reducing Ureteral Stent Related Symptoms
NCT06966804 ·Status: RECRUITING ·Phase: PHASE3
-
(Phosphodiesterase 5 Inhibitors & α-blockers): Single Versus Combined Therapy in Benign Prostatic Hyperplasia
NCT05236634 ·Status: UNKNOWN ·Phase: NA
-
Clinical Progression and Costs in Benign Prostatic Hyperplasia Patients Treated With Early Versus Delayed Combination Therapy
NCT01435954 ·Status: COMPLETED
-
Treatment of Refractory Urinary Retention Secondary to Benign Prostatic Hyperplasia (BPH) With Dual Five Alpha Reductase Inhibition Combined With an Alpha Blocker
NCT00680680 ·Status: COMPLETED ·Phase: NA
-
A Comparative Study of KSO-0400 in BPH Patients With LUTS
NCT01222650 ·Status: COMPLETED ·Phase: PHASE2
-
Study to Compare the Efficacy and Safety of Combination Treatment With Dutasteride and Tamsulosin With Tamsulosin Monotherapy, in Men With Moderate to Severe Benign Prostatic Hyperplasia
NCT02058368 ·Status: COMPLETED ·Phase: PHASE3
-
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
-
Comparison Between Alpha Blocker Monotherapy and 5ARI Monotherapy Following Combination Therapy in Benign Prostatic Hyperplasia (BPH)
NCT01301599 ·Status: COMPLETED ·Phase: PHASE4
-
Efficacy and Safety of Silodosin on Nocturia for Patients With Benign Prostatic Hyperplasia
NCT02106182 ·Status: COMPLETED ·Phase: PHASE4
-
An Observational Study of Dutasteride and Alpha-blocker Combination Therapy in Men With Symptomatic Benign Prostatic Hyperplasia and PSA Level Over 4 ng/mL
NCT01351987 ·Status: UNKNOWN
-
Evaluating the Impact of Early Versus Delayed 5 Alpha Reductase Inhibitor Treatment on the Risk of Emergent Surgery in Men With Benign Prostatic Hyperplasia
NCT01332487 ·Status: COMPLETED
-
Efficacy and Safety of Tadalafil, Tamsulosin, and Their Combinations in Treating Lower Urinary Tract Symptoms in BPH Patients with Prostate Volumes ≤ 40 Ml: a Prospective Comparative Study
NCT06809205 ·Status: COMPLETED ·Phase: PHASE4
-
Benign Prostatic Hyperplasia Trial With Dutasteride And Tamsulosin Combination Treatment
NCT00090103 ·Status: COMPLETED ·Phase: PHASE3
-
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
-
Dutasteride With Tolterodine ER or Placebo to Treat Lower Urinary Tract Symptoms (LUTS)
NCT00939120 ·Status: COMPLETED ·Phase: PHASE4
-
The Use of REZUM System in Chinese Male Patients With LUTS Secondary to Benign Prostate Enlargement
NCT04340934 ·Status: TERMINATED ·Phase: NA
-
Safety and Efficacy of 0.5mg Dutasteride and 0.4mg Tamsulosin Combination Once Daily for Six Months for Benign Prostatic Hyperplasia
NCT01673490 ·Status: TERMINATED ·Phase: PHASE4
-
MCS in Treating Lower Urinary Tract Symptoms (LUTS) Suggestive of Benign Prostatic Hyperplasia
NCT00501371 ·Status: TERMINATED ·Phase: PHASE3
-
Cetrorelix Pamoate in Patients With Symptomatic Benign Prostatic Hypertrophy (BPH)
NCT00663858 ·Status: COMPLETED ·Phase: PHASE3
-
A Phase II Clinical Trial to Evaluate the Efficacy and Safety of GV1001 in Patients With BPH
NCT02855892 ·Status: COMPLETED ·Phase: PHASE2
-
Tadalafil Daily Used Post Turp
NCT06788704 ·Status: COMPLETED
-
Effects of Chronic Use of Doxazosin in Men With Benign Prostatic Hyperplasia
NCT00730418 ·Status: COMPLETED ·Phase: NA
-
Clinical Trial To Evaluate the Efficacy and Safety of CKD-397 in Benign Prostatic Hyperplasia Patients
NCT03246880 ·Status: COMPLETED ·Phase: PHASE3
-
Combination Treatment With Doxazosin Plus TolterodineSR 2 mg Versus 4mg in Men With an Overactive Bladder (OAB) and Benign Prostatic Hyperplasia (BPH)
NCT00922506 ·Status: COMPLETED ·Phase: PHASE4
-
Investigating Medication vs. Prostatic Urethral Lift: Assessment and Comparison of Therapies for BPH
NCT04987892 ·Status: RECRUITING ·Phase: PHASE4