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Completed Phase 2 Interventional Results available

Interventional Clinical Trial in Patients in Overactive Bladder With Nocturia in Women

ClinicalTrials.gov ID: NCT01729819

Public ClinicalTrials.gov record NCT01729819. 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 22, 2026, 5:04 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

A Multi-centre, Double-blind, Randomised Trial Investigating the Efficacy and Safety of a Combination Therapy, Desmopressin and Tolterodine, for Treatment of Overactive Bladder With Nocturia in Women

Study identification

NCT ID
NCT01729819
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Ferring Pharmaceuticals
Industry
Enrollment
106 participants

Conditions and interventions

Interventions

  • Tolterodine tartrate extended release capsules Drug
  • Desmopressin orally disintegrating tablets Drug
  • Placebo orally disintegrating tablets Drug

Drug

Eligibility (public fields only)

Age range
18 Years and older
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
Dec 31, 2012
Primary completion
Oct 31, 2014
Completion
Oct 31, 2014
Last update posted
Sep 11, 2018

2013 – 2014

United States locations

U.S. sites
24
U.S. states
14
U.S. cities
22
Facility City State ZIP Site status
NEA Baptist Clinic Jonesboro Arkansas
Lynn Institute of The Ozarks Little Rock Arkansas
Moez Khorsandi, DO Los Angeles California
Urology Group of Southern California Los Angeles California
Riverside Clinical Research Edgewater Florida
Health Awareness, Inc. Jupiter Florida
Pines Clinical Research, Inc. Pembroke Pines Florida
Palm Beach Research Center West Palm Beach Florida
Clinical Research Atlanta Stockbridge Georgia
Northshore Center for Gastroenterology Evanston Illinois
Remedica, LLC Rochester Michigan
The Urological Institute of Northeastern New York Albany New York
Premier Medical Group of the Hudson Valley, P.C. Poughkeepsie New York
Parkhurst Research Organization, LLC Bethany Oklahoma
Philadelphia Clinical Research, LLC Philadelphia Pennsylvania
Medical University of South Carolina Charleston South Carolina
Coastal Carolina Research Center Mt. Pleasant South Carolina
Vanderbilt University Medical Center Nashville Tennessee
Research Across America Dallas Texas
Advances in Health Houston Texas
Pioneer Research Solutions, Inc. Houston Texas
Radiant Research San Antonio Texas
Clinical Research Associates of Tidewater Norfolk Virginia
Seattle Women's: Health, Research, Gynecology Seattle Washington

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 NCT01729819, 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 11, 2018 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01729819 live on ClinicalTrials.gov.

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