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Prostatic Hyperplasia clinical trials

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NCT ID: NCT01957189 Completed - Clinical trials for Prostatic Hyperplasia

This Will be an Open-label, Three-period, Fixed-sequence Study to Evaluate the Drug-drug Interaction, Pharmacokinetics and Safety of Dutasteride and Tamsulosin When Administered Alone and In-combination in Chinese Healthy Male Volunteers. The Study Will Last Approximately Eleven Weeks. Blood Samples

Start date: October 25, 2013
Phase: Phase 1
Study type: Interventional

This will be an open-label, three-period, fixed-sequence study to evaluate the drug-drug interaction, pharmacokinetics and safety of dutasteride and tamsulosin when administered alone and in-combination in Chinese healthy male volunteers.

NCT ID: NCT01952912 Completed - Clinical trials for Benign Prostate Hyperplasia

Plasmakinetic Enucleation of the Prostate and Open Prostatectomy to Treat Large Prostates

Start date: January 2004
Phase: N/A
Study type: Interventional

The investigators hypothesize that Plasmakinetic Enucleation of the Prostate (PkEP) might yield functional results comparable to OP but with lower perioperative morbidity, and have equivalent long-term efficacy with OP for large prostates. The first objective was to demonstrate the non-inferiority of PKEP compared to OP concerning Qmax at one year postoperatively. To explore the long-term efficacy, we compared the efficacy, safety, and morbidity of PkEP with those of OP in BPH patients with prostate glands larger than 100 g over a follow-up period of 6 years.

NCT ID: NCT01942551 Completed - Clinical trials for Benign Prostate Hyperplasia

Safety and Pharmacokinetic Interaction Study of Tadalafil and Dutasteride

Start date: September 2013
Phase: Phase 1
Study type: Interventional

This is an open-label, two-arm, one-sequence, cross-over study to evaluate the safety and pharmacokinetic interaction after oral concomitant administration of tadalafil and dutasteride in healthy male volunteers.

NCT ID: NCT01939184 Completed - Clinical trials for Benign Prostatic Hyperplasia

Assess Safety & Efficacy of WC3055 in Men With Lower Urinary Tract Symptoms Secondary to Benign Prostatic Hyperplasia

Start date: August 2013
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the safety and efficacy of various fixed daily doses of WC3055 compared with placebo for the treatment of subjects with LUTS secondary to BPH.

NCT ID: NCT01937871 Completed - Clinical trials for Erectile Dysfunction

A Study of Tadalafil in Men With Benign Prostatic Hyperplasia (BPH) and Erectile Dysfunction (ED)

Start date: September 2013
Phase: Phase 3
Study type: Interventional

The purpose of this study is to see whether tadalafil can reduce the signs and symptoms in men with Erectile Dysfunction (ED) and Benign Prostatic Hyperplasia-Lower Urinary Tract Symptoms (BPH-LUTS) and improve their quality of life.

NCT ID: NCT01924988 Completed - Clinical trials for Benign Prostatic Hyperplasia

Prostate Embolization for Benign Prostatic Hyperplasia

Start date: August 2013
Phase: Phase 1/Phase 2
Study type: Interventional

This is a Phase I/II investigator sponsored FDA-approved Investigational Device Exemption protocol, with the primary goal of determining the safety of prostatic artery embolization (PAE) for benign prostatic hyperplasia. Our primary goal is to document the frequency of side effects, particularly bladder and rectal complications, which may occur as a result of this procedure. Secondarily, the study will provide preliminary data to determine its effectiveness in diminishing obstructive symptoms associated with BPH.

NCT ID: NCT01922375 Completed - Clinical trials for Lower Urinary Tract Symptoms Associated With Benign Prostatic Hyperplasia

Clinical Trial to Evaluate the Efficacy and Safety of Naftopidil in Male Patients With Lower Urinary Tract Symptoms Associated With Benign Prostatic Hyperplasia

Start date: December 2011
Phase: Phase 4
Study type: Interventional

This study is designed to evaluate the efficacy and safety of Naftopidil in Korean male patients with with lower urinary tract symptoms associated with benign prostatic hyperplasia. The investigators hypothesized that Naftopidil which came onto marcket in Japan would effect in improvement of voiding and storage difficulty. Design: Placebo-controlled, Randomized, Double-blind, Double-dummy, Parallel group, Fixed dose design

NCT ID: NCT01912339 Completed - Clinical trials for Benign Prostatic Hyperplasia

Safety and Efficacy Study for the Treatment of BPH (Enlarged Prostate)

REZUM
Start date: July 2013
Phase: N/A
Study type: Interventional

To evaluate the safety and efficacy of the Rezūm System and assess its effect on urinary symptoms secondary to benign prostatic hyperplasia (BPH).

NCT ID: NCT01892332 Completed - Clinical trials for TURP(Transurethral Resection of Prostate)

The Effective Concentration of Lidocaine With Fentanyl in Lumbar Epidural Anesthesia for Transurethral Resection of Prostate(TURP) in Elderly Patients

Start date: June 2013
Phase: N/A
Study type: Interventional

Epidural lidocaine is widely used in anesthesia for urologic or lower abdominal surgery because of its rapid onset. But the epidural anesthesia using high concentration of lidocaine may cause excessive motor block and unwanted side effects such as nausea, vomiting and hypotension. This is a study to determine the effective concentration of lidocaine with fentanyl in lumbar epidural anesthesia for transurethral resection of prostate in elderly patients.

NCT ID: NCT01886547 Completed - Prostate Cancer Clinical Trials

2013 Annual National Digital Rectal Exam (DRE) Day Study

Start date: June 2013
Phase: N/A
Study type: Observational [Patient Registry]

We aim to determine the effectiveness of 2013 "Mag paDRE ka" programme in increasing general public awareness on prostate health and promoting prostate health assessment among Filipino males aged 40 or older.