Nocturnal Enuresis Clinical Trial
Official title:
An Open Label, Multi-national Study of Oral Desmopressin in Previously Untreated Children Aged 5 to 15 Years With Primary Nocturnal Enuresis
To evaluate the overall response to desmopressin treatment among previously untreated
enuretic children aged 5-15 years after 3 and 6 months of treatment.
To investigate the influence of possible predictive factors on response after 3 and 6 months
of treatment.
To evaluate the proportion of patients achieving dryness. To evaluate the long-term safety
profile of oral desmopressin in children with primary nocturnal enuresis.
To evaluate the overall response to desmopressin treatment among previously untreated
enuretic children aged 5-15 years after 3 and 6 months of treatment.
To investigate the influence of possible predictive factors on response after 3 and 6 months
of treatment.
To evaluate the proportion of patients achieving dryness. To evaluate the long-term safety
profile of oral desmopressin in children with primary nocturnal enuresis.
;
Allocation: Randomized, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
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