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

ProstaPlant Urology System

Status and phase: Unknown; Phase 1

Conditions: Benign Prostatic Hyperplasia

Treatments: Device: ProstaPlant Stent

Study type: Interventional

Funder types: Industry

Identifiers

NCT00468026

Human Ex-Vivo - V001-3.2007

Details and patient eligibility

About

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.

Sex: Male

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Males,
• 18 years old and up,
• Suffer from BPH,
• Candidate for radical prostatectomies

Exclusion criteria

• According to the physician's decision

Trial design

Primary purpose: Treatment

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)