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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 Oct 22, 2026, 9:24 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 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

Brief summary

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

The purpose of the trial is to investigate the efficacy of combining tolterodine and desmopressin compared with tolterodine monotherapy in the treatment of women with overactive bladder with nocturia in terms of reduction of nocturnal voids during 3 months of treatment

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

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
Jan 2013 (Type not available)
Primary completion
Nov 2014 (Actual)
Completion
Nov 2014 (Actual)
Last update posted
Sep 12, 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 12, 2018 · Synced Oct 22, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01729819 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →