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

ProstaPlant Urology System Ltd.

Overview

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.

Study Type

INTERVENTIONAL

Allocation

Purpose

TREATMENT

Masking

NONE

Conditions

Benign Prostatic Hyperplasia

Interventions

ProstaPlant StentDEVICE

Eligibility

Sex: MALEMin age: 18 Years

Medical Language ↔ Plain English

Inclusion Criteria: * Males, * 18 years old and up, * Suffer from BPH, * Candidate for radical prostatectomies Exclusion Criteria: * According to the physician's decision

Locations (1)

"Asuta" Medical Center

Tel Aviv, Israel

Outcomes

Primary Outcomes

This is a feasibility study, in which initial evaluation of stent insertion procedure is obtained

Central Contacts

Jack Baniel, Prof.

CONTACT

972-3-9376563

Data from ClinicalTrials.gov

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