Viewing Study NCT01779466


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Ignite Modification Date: 2025-12-28 @ 5:26 PM
Study NCT ID: NCT01779466
Status: TERMINATED
Last Update Posted: 2015-04-27
First Post: 2013-01-23
Is NOT Gene Therapy: True
Has Adverse Events: False

Brief Title: Daytime Impact Sleep Study
Sponsor: Ferring Pharmaceuticals
Organization:

Study Overview

Official Title: A Double-blind, Randomised, Parallel-group Trial Investigating Sleep Behaviour and Daytime Performance in Nocturia Patients Treated With Desmopressin Orally Disintegrating Tablets as Compared to Placebo
Status: TERMINATED
Status Verified Date: 2015-04
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Terminated due to lack of eligible patients
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: DAISS
Brief Summary: This trial will investigate the relationship of sleep, daytime performance and nocturia in patients treated with Desmopressin or placebo. Male and Female patients will be administered Desmopressin or Placebo every day for 3 months.
Detailed Description: None

Study Oversight

Has Oversight DMC: False
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?:

Secondary ID Infos

Secondary ID Type Domain Link View
2012-004388-34 EUDRACT_NUMBER None View