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Prostatic Hyperplasia clinical trials

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NCT ID: NCT03064282 Not yet recruiting - Clinical trials for Prostatic Hyperplasia

Prostatic Hyperplasia Treatment and Cancer Prevention

Start date: June 30, 2021
Phase: Early Phase 1
Study type: Interventional

Treatment of patients with prostatic hyperplasia with topical papaverine.

NCT ID: NCT02496442 Not yet recruiting - Clinical trials for Prostatic Hyperplasia

Aqueduct Irrigation System Clinical Protocol: Medical Device Investigational Plan

Start date: July 2015
Phase: N/A
Study type: Interventional

A. Synopsis 1. This protocol comes to direct the experiment to be performed on the Aqueduct Automatic Continuous Irrigation system. 2. The Aquaduct System is aimed at reducing risks to the patient by decreasing the irrigation fluid pressure he may be exposed to, reducing the procedure time and therefore the anesthesia time, reducing the manual handling of the sterile bags and the risk of contamination and more. 3. In general since there is no new procedure suggested and the equipment does not actually come into contact with the human body in any direct way, there is no need to have a clinical study for the regulation purpose. The reason for performing this experiment is to demonstrate the new system and to find out the best way to operate it in order to improve the process and reduce risks. 4. This information will serve the development of most suitable automation solution for achieving the long desired continuous irrigation. 5. The experiment will be performed in the OR in MIS procedures, and will replace the standard gravitational manual method of performing the irrigation. The surgeons and the medical staff of the OR will be directed with the set up and operation of the system prior to using it. The experiment will be accompanied at all times with a knowledgeable representative of the research originator. 6. A maximum of 30 procedures will be analyzed during a period of approximately one month. The surgeons and the medical staff will report their impression of using the system during the procedures and will recommend the best settings achieved. This information will be used to improve the system performance and design.

NCT ID: NCT02279615 Not yet recruiting - Overactive Bladder Clinical Trials

Efficacy And Safety Of Combination Therapy For Treatment Of Overactive Bladder In Male Patients With Benign Prostatic Hyperplasia.

Start date: December 2021
Phase: Phase 4
Study type: Interventional

The purpose of this study is to investigate the safety and efficacy of combination therapy involving β3-adrenoceptor agonist, mirabegron, and α-blockers for the treatment of OAB symptoms in male patients with BPH.

NCT ID: NCT02033798 Not yet recruiting - Clinical trials for Prostatic Hyperplasia

The Effect of Daily Tamsulosin 0.2mg Administration on Renal Function in Patients With Benign Prostatic Hyperplasia

Start date: February 2014
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether medical treatment for bladder outlet obstruction is effective in improvement of glomerular filtration rate and/or proteinuria.

NCT ID: NCT02033785 Not yet recruiting - Clinical trials for Prostatic Hyperplasia

Functional Changes of Urogenital System After Holmium Laser Prostatectomy

Start date: February 2014
Phase: N/A
Study type: Observational [Patient Registry]

Holmium laser prostatectomy will enhance voiding function. Holmium laser prostatectomy will enhance sleep quality. Holmium laser prostatectomy will enhance renal function. Holmium laser prostatectomy will enhance erectile function. Holmium laser prostatectomy will enhance the health-related quality of life.

NCT ID: NCT01876836 Not yet recruiting - Clinical trials for Prostate Hyperplasia

Clasic Laryngeal Mask Airway(C-LMA) and I-gel Releated Regurgitation and Complications

C-LMA
Start date: July 2013
Phase: Phase 4
Study type: Interventional

1. i-gel 2. C-LMA Compare the effect on gastroeosephageal reflux Postoperative complicatios.

NCT ID: NCT01861041 Not yet recruiting - Clinical trials for Benign Prostate Hyperplasia

Low Dose Bupivacaine Spinal for Trans Uretral Prostatectomy.

TURP
Start date: May 2013
Phase: Phase 4
Study type: Interventional

Spinal anesthesia, is used during the transuretheral resection of the prostate.Low dose hyperbaric local anesthetics have been used to enhance the resolution of the spinal block. We compared the efficacy and duration of the spinal block with two different bupivacaine baricities. - Group I: low dose isobaric group - GroupII: Low dose hyperbaric group

NCT ID: NCT01404637 Not yet recruiting - Clinical trials for Benign Prostatic Hyperplasia

Effects of Tamsulosin 0.4mg on Clinical Outcomes in Korean Men With Severe Symptomatic Benign Prostatic Hyperplasia (BPH)

Start date: July 2011
Phase: N/A
Study type: Interventional

The purpose of this study is to compare the efficacy and safety of tamsulosin 0.4mg (Harnal® D. 0.2mg, 2T) with tamsulosin 0.2mg (Harnal® D 0.2mg, 1T) in patients with severe symptomatic benign prostatic hyperplasia as a first line therapy.

NCT ID: NCT01314456 Not yet recruiting - Prostate Cancer Clinical Trials

3D Recording of a Trans-rectal Prostate Biopsy

Start date: March 2011
Phase: N/A
Study type: Interventional

Prostate biopsy is performed by multiple consecutive biopsy needle insertion into the prostate gland under a trans-rectal ultrasound probe guidance. Today, the performing physician navigates the needle using a momentary 2D ultrasound image (longitudinal and transverse B mode) without any record of the full prostate boundaries or previous biopsies' location. This study's Objectives are to record the trans-rectal biopsy procedure including the initial scan and the needle biopsy location and to modulate a 3D model of the prostate with accurate display the locations of the various biopsies taken during the procedure.

NCT ID: NCT00468026 Not yet recruiting - Clinical trials for Benign Prostatic Hyperplasia

Evaluation of the ProstaPlant Prostate Stent Insertion in Ex Vivo Human Prostate

Start date: n/a
Phase: Phase 1
Study type: Interventional

The purpose of this ex-vivo study is to evaluate the insertion procedure for the ProstaPlant implant in human prostates and the support that it supplies to the prostate.