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Completed Phase 3 Interventional Results available

Investigation of the Superiority Effect of Desmopressin to Placebo in Terms of Night Voids Reduction in Nocturia Adult Female Patients

ClinicalTrials.gov ID: NCT01223937

Public ClinicalTrials.gov record NCT01223937. 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, Randomised, Double-blind, Placebo-controlled, Parallel-group Trial to Demonstrate the Efficacy and Safety of Desmopressin Orally Disintegrating Tablet for the Treatment of Nocturia in Adult Females

Study identification

NCT ID
NCT01223937
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Ferring Pharmaceuticals
Industry
Enrollment
268 participants

Conditions and interventions

Conditions

Interventions

  • Desmopressin Drug
  • Placebo 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
Oct 31, 2010
Primary completion
Oct 31, 2011
Completion
Oct 31, 2011
Last update posted
Oct 14, 2015

2010 – 2011

United States locations

U.S. sites
41
U.S. states
20
U.S. cities
39
Facility City State ZIP Site status
Medical Affiliated Research Center Inc. Huntsville Alabama
Radiant Research Inc. Scottsdale Arkansas
Family Medical Center Foothill Ranch California
Axis Clinical Trials Los Angeles California
Radiant Research Inc. Santa Rosa California
Downtown Woman's Health Care Denver Colorado
Front Range Clinical Research Wheat Ridge Colorado
South Florida Medical Research Aventura Florida
Women's Medical Research Group, LLC Clearwater Florida
Avail Clinical Research, LLC DeLand Florida
FPA Clinical Research Kissimmee Florida
Sunrise Medical Research Lauderdale Lakes Florida
DMI Research Pinellas Park Florida
Southeastern Institute Columbus Georgia
Southeastern Medical Research Institute Columbus Georgia
Radiant Research Inc. Chicago Illinois
NorthShore University HealthSystem Evanston Illinois
Accelovance Peoria Illinois
Accelovance South Bend Indiana
FutureCare Studies Springfield Massachusetts
Bay State Clinical Trials, Inc. Watertown Massachusetts
Beyer Research Paw Paw Michigan
Remedica, LLC Rochester Michigan
Radiant Research, Inc. Edina Minnesota
Radiant Research, Inc. St Louis Missouri
Radiant Research Las Vegas Nevada
Anderson & Collins Clinical Research Inc Edison New Jersey
ACCUMED Research Associates Garden City New York
Center for Urologic Research of WNY, LLC Williamsville New York
Radiant Research, Inc. Akron Ohio
Community Research Cincinnati Ohio
Complete HealthCare for Women Columbus Ohio
HWC Women's Research Center Englewood Ohio
Urologic Consultants of SE PA Bala-Cynwyd Pennsylvania
Philadelphia Clinical Research, LLC Philadelphia Pennsylvania
Radiant Research, Inc. Greer South Carolina
Carolina Urologic Research Center Myrtle Beach South Carolina
Radiant Research Inc. Dallas Texas
Quality Research, Inc. San Antonio Texas
Radiant Research, Inc. San Antonio Texas
Exemplar Research Inc. Morgantown West Virginia

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 4 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01223937, 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 Oct 14, 2015 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01223937 live on ClinicalTrials.gov.

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