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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 Oct 23, 2026, 5:42 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

Brief summary

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

A multicenter, randomized, double-blind, placebo-controlled, parallel-group trial to investigate the safety and efficacy of desmopressin oral melt tablets against placebo during 3 months of treatment in adult females with nocturia.

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

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
Nov 2010 (Type not available)
Primary completion
Nov 2011 (Actual)
Completion
Nov 2011 (Actual)
Last update posted
Oct 15, 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 15, 2015 · Synced Oct 23, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01223937 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →