A Study of Minirin Melt in Patients With Nocturia

This is a confirmation of safety profile for Minirin Melt in clinical practice.

Completed

Looking for future studies?

Key information

Conditions

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

Age range

18 year–64 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Private Ambulance, Blansko, Czechia

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

patients suffering from Nocturia

Exclusion criteria

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

Treatment and study plan

Primary outcomes

Number of participants with adverse events

Time frame: 12 months

Secondary outcomes

Number of participants with nocturnal voiding

Time frame: 12 months
Number of participants with adverse events

Time frame: 12 months

Sponsors and collaborators

Lead sponsor

Ferring Pharmaceuticals

Industry

Registry information

Official study title

Minirin Melt Tolerance With Nocturia in the Common Practice Conditions in Czech Republic

Important dates

Study start: 2008
Primary completion: 2010
Study completion: 2011
First posted: Oct 18, 2010
Registry last updated: Oct 8, 2012

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