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Completed Phase 3 Interventional Results available

Investigation of the Superiority Effect of Orally Disintegrating Desmopressin Tablets to Placebo in Terms of Night Voids Reduction in Nocturia Adult Male Patients

ClinicalTrials.gov ID: NCT01262456

Public ClinicalTrials.gov record NCT01262456. 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, 6:15 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, Randomised, Double-blind, Placebo-controlled, Parallel-group Trial With an Open-label Extension to Demonstrate the Efficacy and Safety of Desmopressin Orally Disintegrating Tablets for the Treatment of Nocturia in Adult Males

Study identification

NCT ID
NCT01262456
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Ferring Pharmaceuticals
Industry
Enrollment
395 participants

Conditions and interventions

Conditions

Interventions

  • Desmopressin Drug
  • Placebo Drug

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
Male
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 31, 2011
Primary completion
Dec 31, 2011
Completion
Dec 31, 2011
Last update posted
Oct 14, 2015

2011 – 2012

United States locations

U.S. sites
51
U.S. states
22
U.S. cities
48
Facility City State ZIP Site status
Pinnacle Research Group, LLC Anniston Alabama
Medical Affiliated Research Center, Inc. Huntsville Alabama
Radiant Research, Inc. Scottsdale Arizona
Premiere Pharmaceutical Research Tempe Arizona
Family Medical Center Foothill Rance California
Axis Clinical Trials Los Angeles California
Radiant Research, Inc. Santa Rosa California
Genitourinary Surgical Consultants Denver Colorado
Radiant Research, Inc. Denver Colorado
Front Range Clinical Research, LLC Wheat Ridge Colorado
Connecticut Clinical Research Center, LLC Middlebury Connecticut
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
Advanced Pharma CR, LLC Miami Florida
DMI Research Pinellas Park Florida
Pinellas Urology, Inc St. Petersburg Florida
Midtown Medical Center Tampa Florida
Advanced Research Institute, Inc. Trinity Florida
Radiant Research, Inc. Atlanta Georgia
Southeastern Medical Research Institute Columbus Georgia
Radiant Research, Inc. Chicago Illinois
Accelovance Peoria Illinois
Accelovance South Bend Indiana
FutureCare Studies, Inc. Springfield Massachusetts
Bay State Clinical Trials, Inc. Watertown Massachusetts
Beyer Research Kalmazoo 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
Urology Center Research Institute Englewood New Jersey
AccuMed Research Associates Garden City New York
University Urology Associates New York New York
Radiant Research, Inc. Akron Ohio
Community Research Cincinnati Ohio
Complete HealthCare Columbus Ohio
Urologic Consultants of SE PA Bala-Cynwyd Pennsylvania
Penn Urology Philadelphia Pennsylvania
Hartwell Research Group, LLC Anderson South Carolina
Medical University of South Carolina Charleston South Carolina
Radiant Research, Inc. Greer South Carolina
Carolina Urologic Research Center Myrtle Beach South Carolina
ClinSearch, LLC Chattanooga Tennessee
Radiant Research Inc. Dallas Texas
Quality Research Incorporated San Antonio Texas
Radiant Research, Inc. San Antonio Texas
Wilford Hall Medical Center 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 5 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01262456, 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 23, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01262456 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →