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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 Oct 29, 2026, 4:51 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

Brief summary

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

The purpose of this trial was to confirm/establish long-term safety and efficacy of desmopressin orally disintegrating tablets at dose levels of 50 μg and 75 μg and to further evaluate the safety of an efficacious higher dose level of 100 μg in males with nocturia.

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

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
Feb 2011 (Type not available)
Primary completion
Jan 2012 (Actual)
Completion
Jan 2012 (Actual)
Last update posted
Oct 15, 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 15, 2015 · Synced Oct 29, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01262456 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →