Tamsulosin |
Flomax |
Tamsulosin Systematic (IUPAC) name (R)-5-(2-(2-(2-ethoxyphenoxy)ethylamino)propyl)- 2-methoxybenzenesulfonamide Identifiers CAS number 106133-20-4 ATC code G04CA02 PubChem 129211 DrugBank APRD00036 Chemical data Formula C20H28N2O5S Mol. weight 408.51 Pharmacokinetic data Bioavailability 100% (oral) Metabolism hepatic Half life 9–13 hours Excretion 76% renal Therapeutic considerations Pregnancy cat. B2 (Aust) Legal status Schedule 4 (Aust) POM ( ...
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Tamsulosin Clinical Trials
- Benign Prostatic Hyperplasia Trial With Avodart And Tamsulosin Combination Treatment
ClinicalTrials.gov Identifier: NCT00090103 - Active, not recruiting
Benign Prostatic Hyperplasia
- A Phase 4 Study With Tamsulosin OCAS to Assess Nighttime Voiding.
ClinicalTrials.gov Identifier: NCT00379067 - Active, not recruiting
Benign Prostatic Hyperplasia
- A Study to Evaluate Solifenacin Succinate in Combination With Tamsulosin for the Treatment of Residual Overactive Bladder Symptoms (OAB) in Men.
ClinicalTrials.gov Identifier: NCT00333112 - Active, not recruiting
Urinary Incontinence
- A Study With Combination Treatment (Tamsulosin Hydrochloride and Solifenacin Succinate) in Male Patients With LUTS/BPH
ClinicalTrials.gov Identifier: NCT00510406 - Active, not recruiting
Lower Urinary Tract Symptoms; Prostatic Hyperplasia
- An Effectiveness and Safety Study Comparing Oxybutynin Chloride Plus FLOMAX (Tamsulosin HCl) and Placebo Plus FLOMAX (Tamsulosin HCl) for the Treatment of Lower Urinary Tract Symptoms.
ClinicalTrials.gov Identifier: NCT00338624 - Completed
Urination Disorders
- Efficacy and Safety of SL77.0499-10 (Alfuzosin) Versus Placebo and Tamsulosin in Japanese Patients With Benign Prostatic Hyperplasia
ClinicalTrials.gov Identifier: NCT00399464 - Active, not recruiting
Prostatic Hyperplasia
- Is There is a Role of Prophylactic Therapy With Tamsulosin Before Extracorporeal Shock Wave Lithotripsy to Avoid Development of Steinstrasse ?
ClinicalTrials.gov Identifier: NCT00489723 - Recruiting
Kidney Stones
- Tamsulosin for Urolithiasis in the Emergency Dept
ClinicalTrials.gov Identifier: NCT00382265 - Not yet recruiting
Nephrolithiasis
- The Efficacy of Tamsulosin in the Treatment of Ureteral Stones in Emergency Department Patients
ClinicalTrials.gov Identifier: NCT00448123 - Recruiting
Kidney Stones; Uretral Stones
- Evaluation of Tamsulosin in the Treatment of Ureteral Stones
ClinicalTrials.gov Identifier: NCT00151567 - Completed
Ureterolithiasis; Ureteral Calculi
- PK/PD, Long-Term Safety and Efficacy of Tamsulosin Treatment in Children With Neurogenic Bladder
ClinicalTrials.gov Identifier: NCT00340704 - Recruiting
Bladder, Neurogenic
- Study of Tamsulosin and/or Dutasteride to Relieve Urinary Symptoms After Brachytherapy for Localized Prostate Cancer
ClinicalTrials.gov Identifier: NCT00244309 - Recruiting
Prostate Cancer
- Complementary and Alternative Medicine for Urological Symptoms
ClinicalTrials.gov Identifier: NCT00097136 - Recruiting
Prostatic Hyperplasia
- Comparing Patients After ESWL Treated With Ureteral Stents Versus Expulsion Therapy With Tamsulosin
ClinicalTrials.gov Identifier: NCT00478998 - Not yet recruiting
Upper Tract Ureterolithiasis
- Solifenacin Succinate With Tamsulosin HCl in Males With Lower Urinary Tract Symptoms and Bladder Outlet Obstruction
ClinicalTrials.gov Identifier: NCT00507455 - Recruiting
Lower Urinary Tract Symptoms; Bladder Outlet Obstruction
- Phase I Study to Investigate the Drug Interaction After Oral Administration of Tamsulosin and SK3530
ClinicalTrials.gov Identifier: NCT00489606 - Completed
Erectile Dysfunction
- Tamsulosin Phase III Clinical Trial -Double-Blind, Placebo Controlled Study in Female Patients With Lower Urinary Tract Syndrome
ClinicalTrials.gov Identifier: NCT00239265 - Completed
Urinary Tract Diseases
- Tamsulosin Phase III Clinical Trial -Double-Blind, Placebo Controlled Study in Male Patients With Lower Urinary Tract Syndrome
ClinicalTrials.gov Identifier: NCT00239317 - Completed
Urinary Tract Diseases
- Effect and Safety Of Detrol LA In Men With Overactive Bladder Symptoms With Or Without Bladder Outlet Obstruction
ClinicalTrials.gov Identifier: NCT00147654 - Completed
Urinary Incontinence

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