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Not listed Not applicable Interventional Accepts healthy volunteers

Lyrette: Renewing Continence Objective and Subjective Efficacy Study

ClinicalTrials.gov ID: NCT01455779

Public ClinicalTrials.gov record NCT01455779. 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 Jun 26, 2026, 8:02 AM EDT

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

Study identification

NCT ID
NCT01455779
Recruitment status
Not listed
Study type
Interventional
Phase
Not applicable
Lead sponsor
Verathon
Industry
Enrollment
54 participants

Conditions and interventions

Interventions

  • Lyrette Device

Device

Eligibility (public fields only)

Age range
35 Years to 60 Years
Sex
Female
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
Aug 31, 2011
Primary completion
Jun 30, 2015
Completion
Jun 30, 2015
Last update posted
Dec 8, 2014

2011 – 2015

United States locations

U.S. sites
6
U.S. states
5
U.S. cities
6
Facility City State ZIP Site status
Tri Valley Urology Medical Group Murrieta California 92562
Center for Bladder Control Arlington Heights Illinois 60004
Women's Health Institute of Illinois Oak Lawn Illinois 60453
Female Pelvic Medicine and Urogynecology Grand Rapids Michigan 49503
Dial Research, Tennessee Women's Care Nashville Tennessee 37203
Eastern Virginia Medical School Norfolk Virginia 23507

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 NCT01455779, 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 Dec 8, 2014 · Synced Jun 26, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01455779 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →