A Study of Minirin Melt in 24 Months Treatment in Patients With Nocturia

A Confirmation of the Safety Profile for Minirin Melt in Clinical Practice

Completed

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Key information

Conditions

Nocturia Lower Urinary Tract Symptoms Pathological Conditions, Signs and Symptoms Signs and Symptoms Urological Manifestations

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Nemocnice Rudolfa a Stefanie (there may be other sites in this country), Benešov, Czechia

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

nocturia

Exclusion criteria

habitual or psychogenic polydipsia,
known or suspected cardiac insufficiency
other conditions requiring treatment with diuretics
moderate and severe renal insufficiency
known hyponatremia
syndrome of inappropriate ADH secretion

Treatment and study plan

Primary outcomes

Number of patients with adverse events

Time frame: 24 months

Secondary outcomes

Number of changes in dosage regime

Time frame: 24 months

Sponsors and collaborators

Lead sponsor

Ferring Pharmaceuticals

Industry

Registry information

Official study title

A Prospective Safety Study in 24 Months Treatment of Nocturia With Minirin Melt in Clinical Practice in the Czech Republic

Important dates

Study start: 2012
Primary completion: 2016
Study completion: 2016
First posted: Mar 13, 2012
Registry last updated: May 24, 2016

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.

Completed