Evaluation of the ProstaPlant Prostate Stent Insertion in Ex Vivo Human Prostate
NCT00468026 · Status: UNKNOWN · Phase: PHASE1 · Type: INTERVENTIONAL
Last updated 2007-05-01
Summary
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.
Conditions
- Benign Prostatic Hyperplasia
Interventions
- DEVICE
-
ProstaPlant Stent
Sponsors & Collaborators
-
ProstaPlant Urology System Ltd.
lead INDUSTRY
Principal Investigators
-
Jack Baniel, Prof. · "Rabin" Medical Center - "Belinson" Campus - Urology Department
Study Design
- Allocation
- NA
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 18 Years
- Sex
- MALE
- Healthy Volunteers
- No
Timeline & Regulatory
Countries
- Israel
Study Locations
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