An observational study in Nocturia, sponsored by Ferring Pharmaceuticals. Completed at 37 sites in Czechia. Open to participants aged 18 Years to 64 Years. Per ClinicalTrials.gov, last updated 2012-10-08.
Sponsored by Ferring Pharmaceuticals · Observational
This is a confirmation of safety profile for Minirin Melt in clinical practice.
126 studies on the registry are indexed under Nocturia; 24 are open to participants now.
This study's enrollment of 588 is above the median of 275 across 26 observational studies indexed under Nocturia.
Browse Nocturia studies →Ferring Pharmaceuticals is the lead sponsor of 249 studies on the registry; 4 are open to participants now.
Of its 15 completed or terminated interventional studies of FDA-regulated products, 14 (93%) have results posted.
Counted across the registry records on this site, refreshed daily.
Primary care clinic
Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.
Exclusion Criteria:
Number of participants with adverse events
Time frame: 12 months
Number of participants with nocturnal voiding
Time frame: 12 months
Number of participants with adverse events
Time frame: 12 months
This study is completed, as verified in Oct 2012. You cannot join it, but the record below documents what was studied.
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