Found 106 matching trials
FLOMAX® Versus HYTRIN® in Patients With the Signs and Symptoms of Benign Prostatic Hyperplasia PHASE4 1. To study the early onset of symptomatic relief afforded by FLOMAX® capsu...
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Multiple Locations
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Advanced Benefits of Alpha-blocker Monotherapy on Lower Urinary Tracts Symptoms(LUTS) Patients PHASE4 The purpose of this study is to evaluate the clinical efficacy of alpha-blo...
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Soon Chun Hyang University Hospital Cheonan
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Peri-operative Tamsulosin and Impact on Voiding Trial After Same-day Urogynecology Surgery PHASE3 The purpose of this research study is to determine if taking tamsulosin pre...
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Use of Tamsulosin to Reduce the Incidence and Duration of Postoperative Urinary Retention Following Spine Surgery PHASE3 Postoperative urinary retention is a frequent complication of spinal surger...
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Mayo Clinic in Rochester
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Double j Stent Related Symptoms EARLY_PHASE1 In urology, ureteral stents are used to treat obstructive diseases. Hematur...
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Elsayed Abdelhalim
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Tamsulosin With or Without Tadalafil for Trial Without Catheter After Acute Urinary Retention Due to Benign Prostatic Hyperplasia PHASE4 Acute urinary retention is a common emergency in men with benign prostatic ...
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Department of Urology- Beni-Suef University Hospitals
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Efficacy of Mirabegron Versus Tamsulosin Versus Solifenacin for Treatment of Ureteral Stents-Related Symptoms PHASE3 The primary objective of this prospective, single-centre randomized control...
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Urology and Nephrology Center
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Tamsulosin as Adjuvant Treatment Prior to Endoscopic Ureterolithotomy PHASE4 This a study aiming to compare treatment with tamsulosin versus placebo in ...
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Hospital Clinico Pontificia Universidad católica de Chile
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The Effect of Tamsulosin on Postoperative Urinary Retention PHASE4 This is a double-blinded randomized controlled trial of perioperative use o...
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Wake Forest Health Sciences
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A Study of Tadalafil in Men With Benign Prostatic Hyperplasia PHASE3 The purpose of this study is to determine whether an experimental drug know...
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For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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