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NCT02710422 · ClinicalTrials.gov registry record · Phase 2

Miami Membrane for Potency (MMEP) Trial

A Phase 2 study, sponsored by University of Miami.

Terminated
Registry status
Phase 2
Development phase
24
Enrollment target

NCT02710422: Clinical Trial Phase 2 study, sponsored by University of Miami.

NCT02710422 is a Phase 2 study that was terminated before completion, run by University of Miami. The registered enrollment target is 24 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (82% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02710422, a Phase 2 study, was terminated before completion, sponsored by University of Miami.

TERMINATED
Registry status
Phase 2
Development phase
24 participants
Enrollment target

Study Summary

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.

Primary Outcome

The difference in average change in Sexual History Inventory for Men (SHIM) score, between baseline and 12 months post RARP between the membrane and control arms will be assessed as the primary endpoint. The SHIM score is measured in points on a scale: The minimum score is 5 to 7 indicating severe erectile dysfunction (ED), the maximum score is 22 to 25, indicating no ED.

Interventions

  • BIOLOGICAL Amniotic Membrane Placement
  • BEHAVIORAL EPIC 26
  • OTHER PSA Measurement
  • BEHAVIORAL Sexual History Inventory for Men

Trial Details

FieldValue
Enrollment Target 24 participants
Start Date 2016-05-17
Est. Completion 2019-01-22
Phase Phase 2
University of Miami

721 total trials

Why NCT02710422 stopped before completion

NCT02710422 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 24 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (82% lower).

The record links to 0 conditions, and to 4 interventions - of which Amniotic Membrane Placement is the first listed.

NCT02710422 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02710422 about?

NCT02710422 is a clinical study titled "Miami Membrane for Potency (MMEP) Trial". 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.

What is the current status of trial NCT02710422?

This trial is currently terminated. It is a Phase 2 study. The enrollment target is 24 participants. The study started on 2016-05-17. Estimated completion is 2019-01-22.

What interventions are being tested in trial NCT02710422?

The interventions under investigation include: Amniotic Membrane Placement (BIOLOGICAL), EPIC 26 (BEHAVIORAL), PSA Measurement (OTHER), Sexual History Inventory for Men (BEHAVIORAL).

Who is sponsoring clinical trial NCT02710422?

This trial is sponsored by University of Miami, which has 721 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02710422's enrollment target sits among peer trials

24 1756th of 2000 higher than 217 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT02710422, the US trial registry maintained by the National Library of Medicine. NCT02710422 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.