Prostate Cancer Clinical Trial
Official title:
Miami Membrane for Potency (MMeP) Trial to Assess the Impact of Dehydrated Human Amnion Membrane Allograft Placement During Robotic Radical Prostatectomy on Early Return of Erectile Function
The use of dehydrated human amnionic membrane allograft improves erectile function recovery (as measured by (Sexual History Inventory for Men (SHIM) score) at 12 months after robotic assisted radical prostatectomy (RARP) compared to a control group with no allograft.
This is a phase 2 prospective randomized trial investigating the impact of amniotic membrane
placement over the neurovascular bundles after bilateral nerve sparing robot assisted radical
prostatectomy on potency. The study will have a control arm that will follow standard of care
surgery, without placement of any membranes. 70 men will be allocated to each arm.
The research study will involve follow up every 3 months for the first 12 months. After this
the investigators will follow patients annually with prostate-specific antigen (PSA)
measurements and an assessment of any secondary therapies for 5 years post-surgery.
Randomization of study patients will be done in equal proportion to Arm I (membrane
placement) and Arm II (no membrane placement, standard of care surgery) using a permuted
block design stratified by baseline SHIM score (<17 vs. >=17), and use of ANY erectile aids
(Yes vs. No) in the last 3 months.
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