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Completed Phase 2 Interventional

MILADY: A Randomized, Placebo-controlled Safety and Efficacy Trial of SSR240600C in Treatment of Overactive Bladder or Urge Urinary Incontinence.

ClinicalTrials.gov ID: NCT00174798

Public ClinicalTrials.gov record NCT00174798. 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 Jul 23, 2026, 5:29 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-blind, Placebo and Active-controlled Efficacy and Safety Study of SSR240600C in Patients With Overactive Bladder (OAB) or Urge Urinary Incontinence (UUI)

Study identification

NCT ID
NCT00174798
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Sanofi
Industry
Enrollment
118 participants

Conditions and interventions

Interventions

  • SSR240600C Drug
  • Placebo Drug
  • Tolterodine Drug

Drug

Eligibility (public fields only)

Age range
18 Years to 75 Years
Sex
Female
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
Apr 30, 2005
Primary completion
Apr 30, 2006
Completion
Apr 30, 2006
Last update posted
Feb 1, 2012

2005 – 2006

United States locations

U.S. sites
22
U.S. states
15
U.S. cities
22
Facility City State ZIP Site status
Hope Research LLC Phoenix Arizona 85032
Research Tuscon Tuscon Arizona 85712
Medical Center for Clinical Research San Diego California 92108
Genitourinary Surgical Consultants Denver Colorado 80220
Connecticut Clinical Research Center, Urology Specialists Waterbury Connecticut 06708
Miami Research Associates Miami Florida 33143
Southeastern Research Group Tallahassee Florida 32308
Atlanta Women's Research Institute Alpharetta Georgia 30005
Mount Vernon Clinical Research Atlanta Georgia 30328
Soapstone Center for Education & Clinical Research Decatur Georgia 30034
Urology of Indiana Greenwood Indiana 46143
Metropolitan Urology Jeffersonville Indiana 47130
Rockhill Medical Plaza Kansas City Missouri 64131
Hudson Valley Urology Center Kingston New York 12401
Hudson Valley Urology Poughkeepsie New York 12601
Daniel Laury Medford Oregon 97504
Philadelphia Women's Research Philadelphia Pennsylvania 19114
Clinical Trials Research Services Pittsburgh Pennsylvania 15206
University Urological Research Institute Providence Rhode Island 02904
Advanced Research Associates Corpus Christi Texas 78414
Tacoma Women's Specialists Research Tacoma Washington 98405
Midwest Research SpecialistsSt. Michael's Hospital Milwaukee Wisconsin 53209

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 NCT00174798, 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 Feb 1, 2012 · Synced Jul 23, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00174798 live on ClinicalTrials.gov.

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