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Prostatic Hyperplasia clinical trials

View clinical trials related to Prostatic Hyperplasia.

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NCT ID: NCT02737241 Completed - Clinical trials for Prostatic Hyperplasia

HoLEP (50W) vs. HoLEP (100W) for Treatment of BPH

Start date: June 1, 2015
Phase: N/A
Study type: Interventional

HoLEP (Holmium laser enucleation of the prostate) entails dissection of the whole median and lateral prostatic lobes off the surgical capsule via a retrograde approach starting at the apex. The enucleated lobes were pushed to the bladder followed by hemostasis of the prostate bed then intravesical morcellation of the enucleated adenoma. The investigators are going to compare safety and efficacy of low power; LP-HoLEP vs. high power; HP-HoLEP in treatment of infra-vesical obstruction secondary to BPH (Benign prostate Hyperplasia).

NCT ID: NCT02715401 Completed - Clinical trials for Erectile Dysfunction

PK and Safety of HCP1303 and Co-administration of HGP1201, HIP1402 Under Fed Condition in Healthy Male Volunteers

Start date: October 2015
Phase: Phase 1
Study type: Interventional

To investigate the pharmacokinetic properties and safety after administration of HCP1303 and co-administration of HGP1201, HIP1402 under Fed Condition in healthy male volunteers

NCT ID: NCT02712411 Completed - Clinical trials for Erectile Dysfunction

Pharmacokinetics and Safety of HCP1303 and Co-administration of HGP1201, HIP1402 in Healthy Male Volunteers

Start date: July 2015
Phase: Phase 1
Study type: Interventional

To investigate the pharmacokinetic properties and safety after administration of HCP1303 and co-administration of HGP1201, HIP1402 in healthy male volunteers

NCT ID: NCT02689830 Active, not recruiting - Clinical trials for Prostatic Hypertrophy, Benign

Prostate Embolization for Acute Urinary Retention Study

PARIS1
Start date: March 2016
Phase: N/A
Study type: Interventional

The purpose of this study is to assess the feasibility and safety of Prostate Artery Embolization (PAE) in patients suffering of Acute Urinary Retention (AUR) in the context Benign Prostatic Hypertrophy (BPH).

NCT ID: NCT02683980 Active, not recruiting - Clinical trials for Treatment of Benign Prostatic Hyperplasia

Ablation Efficacy of Contact Side Firing Fiber in Predefined Settings for Treating BPH

Start date: February 2016
Phase: N/A
Study type: Interventional

Twenty (20) subjects presenting with a hyperplasia enlarged prostate and candidates for surgery will undergo a single treatment for ablation of the prostate using the study device.Follow up visits are scheduled for the day of release from the hospital and at 1 and 3 months post procedure. The primary objective of this study is to explore Vaporization efficacy and safety when treating PBH (Benign prostatic hyperplasia ) with the contact side firing fiber with recommended settings.

NCT ID: NCT02681471 Completed - Acute Hyponatremia Clinical Trials

Bipolar Versus Monopolar Resection of Benign Prostate Hyperplasia

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

Aim of this prospective clinical study was to compare two different surgical techniques and used solutions on serum electrolytes, bleeding and Transurethral Resection of Prostate (TURP) syndrome undergoing TURP. Fifty-three patients scheduled for elective TURP were enrolled in this prospective clinical study. Patients were included one of two groups (Group Monopolar and Group Bipolar).

NCT ID: NCT02679430 Withdrawn - Clinical trials for Benign Prostatic Hyperplasia

Analysis of Prostatic Arterial Embolization for Benign Prostatic Hyperplasia Using Embosphere Microspheres

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

Investigators hypothesis that arterial embolization of men with symptomatic BPH, analogous to uterine fibroid embolization for women, is safe and effective.

NCT ID: NCT02676544 Terminated - Clinical trials for Lower Urinary Tract Symptoms

Prostate Embolization for Massive Benign Prostatic Hypertrophy (BPH)

Start date: December 2015
Phase: Phase 1/Phase 2
Study type: Interventional

This is a prospective, open label single center feasibility study to demonstrate basic safety and effectiveness of prostate artery embolization for the treatment of symptomatic benign prostatic Hyperplasia (BPH) in a small series of patients with large (≥90 grams) glands.

NCT ID: NCT02667938 Completed - Clinical trials for Benign Prostatic Hyperplasia

A Phase 3 Clinical Trial to Evaluate the Efficacy and Safety of HCP1303 Capsules

Start date: March 2015
Phase: Phase 3
Study type: Interventional

The main objective of this study is to evaluate efficacy and safety of HCP1301 capsule in patients with Benign Prostatic Hyperplasia and Erectile Dysfunction

NCT ID: NCT02656173 Completed - Overactive Bladder Clinical Trials

A Phase 4 Study to Evaluate the Efficacy, Safety, and Tolerability of Mirabegron in Male Subjects With Overactive Bladder (OAB) Symptoms, While Taking the Alpha Blocker for Benign Prostatic Hypertrophy (BPH)

Start date: January 25, 2016
Phase: Phase 4
Study type: Interventional

The primary objective of the study was to investigate the efficacy of mirabegron versus placebo in male patients with OAB symptoms while taking the alpha blocker, tamsulosin, for BPH.