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NCT01715571 · ClinicalTrials.gov registry record · NA

Assessment of Penile Vibratory Stimulation Using the Viberect in Men With Mild-Moderate ED

A NA study, sponsored by Johns Hopkins University.

Terminated
Registry status
NA
Development phase
11
Enrollment target

NCT01715571: Clinical Trial NA study, sponsored by Johns Hopkins University.

NCT01715571 is a NA study that was terminated before completion, run by Johns Hopkins University. The registered enrollment target is 11 participants. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01715571, a NA study, was terminated before completion, sponsored by Johns Hopkins University.

TERMINATED
Registry status
NA
Development phase
11 participants
Enrollment target

Study Summary

The primary objective of this study is to assess the safety, acceptability, and satisfaction of penile vibratory stimulation in treatment of erectile dysfunction (ED). The secondary objective is to demonstrate subjective physiological response (erection, rigidity, orgasm) after four weeks of frequent device use and the satisfaction of penile erection and sexual intercourse with partner.

Interventions

  • DEVICE Viberect

Trial Details

FieldValue
Enrollment Target 11 participants
Start Date 2013-03-01
Est. Completion 2020-07-01
Phase NA

Sponsor

Johns Hopkins University

1,448 total trials

What the Registry Record Tells You About NCT01715571

The ClinicalTrials.gov registry entry for NCT01715571 describes a study currently listed as terminated, categorized as NA. The registered enrollment target is 11 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Johns Hopkins University, which has 1,448 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 1 intervention - of which Viberect is the first listed.

NCT01715571 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT01715571 about?

NCT01715571 is a clinical study titled "Assessment of Penile Vibratory Stimulation Using the Viberect in Men With Mild-Moderate ED". The primary objective of this study is to assess the safety, acceptability, and satisfaction of penile vibratory stimulation in treatment of erectile dysfunction (ED). The secondary objective is to demonstrate subjective physiological response (erection, rigidity, orgasm) after four weeks of frequen...

What is the current status of trial NCT01715571?

This trial is currently terminated. It is a NA study. The enrollment target is 11 participants. The study started on 2013-03-01. Estimated completion is 2020-07-01.

What interventions are being tested in trial NCT01715571?

The interventions under investigation include: Viberect (DEVICE).

Who is sponsoring clinical trial NCT01715571?

This trial is sponsored by Johns Hopkins University, which has 1,448 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, the data changelog, or report a data error.