Development of a new patient-reported outcome (PRO) measure on the Impact of Nighttime Urination (INTU) in patients with nocturia-Psychometric validation
Author:
Affiliation:
1. Mercy Health Urogynecology; Norton Shores Michigan
2. Xcenda; Palm Harbor Florida
3. Adelphi Values; Boston Massachusetts
4. Allergan plc; Irvine California
5. Serenity Pharmaceuticals, LLC; Milford Pennsylvania
Funder
Serenity Pharmaceuticals, LLC, Milford, PA, USA
Allergan
Publisher
Wiley
Subject
Urology,Neurology (clinical)
Reference14 articles.
1. Nocturia research: current status and future perspectives;van Kerrebroeck;Neurourol Urodyn,2010
2. The prevalence of nocturia and its effect on health-related quality of life and sleep in a community sample in the USA;Coyne;BJU Int,2003
3. Nocturia in the Dutch adult population;van Dijk;BJU Int,2002
4. The prevalence and causes of nocturia;Bosch;J Urol,2013
5. Desmopressin orally disintegrating tablet effectively reduces nocturia: results of a randomized, double-blind, placebo-controlled trial;Weiss;Neurourol Urodyn,2012
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2. Systematic Review of the Effect of a One-Day Versus Seven-Day Recall Duration on Patient Reported Outcome Measures (PROMs);The Patient - Patient-Centered Outcomes Research;2023-02-14
3. Efficacy and Safety of SER120 Nasal Spray in Patients with Nocturia: Pooled Analysis of 2 Randomized, Double-Blind, Placebo Controlled, Phase 3 Trials;Journal of Urology;2018-09
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