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Completed Phase 3 Interventional

Open-label Study of the Efficacy and Safety of VESIcare® in Patients With Overactive Bladder Symptoms

ClinicalTrials.gov ID: NCT00463541

Public ClinicalTrials.gov record NCT00463541. 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.

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ClinicalTrials.gov public records Last synced Oct 18, 2026, 8:53 PM EDT

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

Official title

An Open-label Study of the Efficacy and Safety of 5 and 10mg VESIcare® (Solifenacin Succinate) in Patients With Overactive Bladder Symptoms VOLT: VESIcare® Open-Label Trial

Brief summary

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

To evaluate the safety and efficacy of solifenacin succinate in subjects with overactive bladder symptoms (urgency, with or without urge incontinence, usually with frequency and nocturia).

Study identification

NCT ID
NCT00463541
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Astellas Pharma Inc
Industry
Enrollment
2,225 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
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
Jun 2004 (Type not available)
Primary completion
Apr 2005 (Actual)
Completion
Apr 2005 (Actual)
Last update posted
Sep 18, 2014

2004 – 2005

United States locations

U.S. sites
198
U.S. states
38
U.S. cities
174
Facility City State ZIP Site status
Not listed Bay Minette Alabama 35607 —
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Not listed Albuquerque New Mexico 87108 —
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Not listed Rochester New York 14609 —
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Not listed Asheboro North Carolina 27205 —
Not listed Cary North Carolina 27511 —
Not listed Charlotte North Carolina 28204 —
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Not listed Columbus North Carolina 28722 —
Not listed Greensboro North Carolina 27401 —
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Not listed Canton Ohio 44708 —
Not listed Cincinnati Ohio 45236 —
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Not listed McConnelsville Ohio 43756 —
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Not listed Bensalem Pennsylvania 19020 —
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Not listed Camp Hill Pennsylvania 17011 —
Not listed Dauphin Pennsylvania 17018 —
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Not listed Phoenixville Pennsylvania 19460 —
Not listed Pittsburgh Pennsylvania 15206 —
Not listed Williamsport Pennsylvania 17701 —
Not listed Mt. Pleasant South Carolina 29464 —
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Not listed Bartlett Tennessee 38134 —
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Not listed Plano Texas 75093 —
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Not listed Salt Lake City Utah 84107 —
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Not listed Charlottesville Virginia 22908 —
Not listed Hampton Virginia 23666 —
Not listed Vienna Virginia 22180 —
Not listed Seattle Washington 98133 —
Not listed Spokane Washington 99204 —
Not listed Tacoma Washington 98450 —
Not listed Huntington West Virginia 25701 —

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 NCT00463541, 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 Sep 18, 2014 · Synced Oct 18, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00463541 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →