Evaluation of the ProstaPlant Prostate Stent Insertion in Ex Vivo Human Prostate
1 other identifier
interventional
N/A
1 country
1
Brief 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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
April 30, 2007
CompletedFirst Posted
Study publicly available on registry
May 1, 2007
CompletedMay 1, 2007
March 1, 2007
April 30, 2007
April 30, 2007
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
This is a feasibility study, in which initial evaluation of stent insertion procedure is obtained
Interventions
Eligibility Criteria
You may qualify if:
- Males,
- years old and up,
- Suffer from BPH,
- Candidate for radical prostatectomies
You may not qualify if:
- According to the physician's decision
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
"Asuta" Medical Center
Tel Aviv, 62748, Israel
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Jack Baniel, Prof.
"Rabin" Medical Center - "Belinson" Campus - Urology Department
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- phase 1
- Allocation
- NA
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- INDUSTRY
Study Record Dates
First Submitted
April 30, 2007
First Posted
May 1, 2007
Last Updated
May 1, 2007
Record last verified: 2007-03