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Completed Phase 2 Interventional

PSD502 in Subjects With Premature Ejaculation

ClinicalTrials.gov ID: NCT03578783

Public ClinicalTrials.gov record NCT03578783. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 21, 2026, 6:46 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Pilot Multicenter, Randomized, Double-Blind Study Comparing The Proportion Of Responders to PSD502 and to Placebo Using the PEBEQ In Subjects With Premature Ejaculation

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This study is being done to test the effect of PSD502 (the study medication) compared to placebo in subjects with premature ejaculation. PSD502 is a topical (applied to skin) anesthetic spray containing a mixture of two drugs called lidocaine and prilocaine that will be applied to the penis. Half of the subjects will receive PSD502 and half will receive placebo.

Study identification

NCT ID
NCT03578783
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Plethora Solutions Ltd
Industry
Enrollment
121 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
Male
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Dec 26, 2018 (Actual)
Primary completion
May 4, 2021 (Actual)
Completion
Dec 1, 2021 (Actual)
Last update posted
Jul 5, 2022

2018 – 2021

United States locations

U.S. sites
21
U.S. states
12
U.S. cities
21
Facility City State ZIP Site status
Achieve Clinical Research Birmingham Alabama 35216 —
Coastal Clinical Research Mobile Alabama 36608 —
Skyline Urology Sherman Oaks California 91411 —
Imagine Research of Palm Beach County Boynton Beach Florida 33435 —
SunCoast Research Miami Florida 33133 —
Suncoast Research Associates Miami Lakes Florida 33014 —
Clinical Research Center of Florida Pompano Beach Florida 33060 —
Primary Care Research Atlanta Georgia 30312 —
Georgia Clinical Research, Llc Lawrenceville Georgia 30044 —
Regional Urology, LLC Shreveport Louisiana 71106 —
Chesapeake Urology Research Associates Towson Maryland 21204 —
Boston Clinical Trials Boston Massachusetts 02131 —
Mens Health Boston Chestnut Hill Massachusetts 02467 —
Jubilee Clinical Research, Inc Las Vegas Nevada 89106 —
Accumed Research Associates Garden City New York 11530 —
Manhattan Medical Research Practice New York New York 10016 —
Premier Medical Group of the Hudson Valley Poughkeepsie New York 12601 —
M3 Wake Research, Inc Raleigh North Carolina 27612 —
Midlantic Urology Bala-Cynwyd Pennsylvania 19004 —
Advanced Clinical Research - Jordan Ridge Family Medicine Salt Lake City Utah 84123 —
Advanced Clinical Research West Jordan Utah 84088 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03578783, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jul 5, 2022 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT03578783 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →