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Terminated Not applicable Interventional Accepts healthy volunteers

Clinical Study to Evaluate the Performance of Synthetic Polyurethane Male Condoms

ClinicalTrials.gov ID: NCT05536336

Public ClinicalTrials.gov record NCT05536336. 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, 2:06 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 Randomized, Double-Blinded, Crossover and Multi-center Clinical Study to Evaluate the Performance of Synthetic Polyurethane Male Condom Compared to Standard Latex Condom During Vaginal Intercourse

Brief summary

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

This study is a randomized, double-blinded, crossover and multi-center study to evaluate the clinical breakage and slippage of a new synthetic polyurethane male condom compared to a commercially available standard latex condom.

Study identification

NCT ID
NCT05536336
Recruitment status
Terminated
Study type
Interventional
Phase
Not applicable
Lead sponsor
Okamoto Industries, Inc.
Industry
Enrollment
188 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 65 Years
Sex
All
Healthy volunteers
Accepts healthy volunteers

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

Study timeline

Start date
Sep 8, 2022 (Actual)
Primary completion
Jul 12, 2023 (Actual)
Completion
Jun 27, 2024 (Actual)
Last update posted
Mar 20, 2025

2022 – 2024

United States locations

U.S. sites
4
U.S. states
4
U.S. cities
4
Facility City State ZIP Site status
Physicians Research Group Mesa Arizona 85209 —
Angels Clinical Research Center Miami Florida 33176 —
Physicians Research Group West Lafayette Indiana 47906 —
Wellnow Cincinnati Ohio 45212 —

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 NCT05536336, 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 Mar 20, 2025 · 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 NCT05536336 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →