Italian multicentre open trial on DDAVP spray in nocturnal enuresis

Objective: The aim of the study was to compare the efficacy and safety of d ifferent doses of DDAVP spray treatment (20 to 40 mcg/day) in patients with primary monosymptomatic nocturnal enuresis (defined as three or more wet n ights per week). Material and Methods: 237 patients (152 males, 75 females; age range 5-17 years), with no infections or organic abnormalities of the urinary apparatus and no neurological disorders, were admitted into the tri al. The experimental design was planned as an "open study" with five differ ent treatments schedules (5 groups). The daily doses of DDAVP at bedtime in groups 1 and 2 were 20 and 30 mcg, respectively, for 6 weeks. In groups 3 and 4 the daily doses for the first 2 weeks were 20 and 30 mcg, respectivel y, and then, after a washout period of 2 weeks, the daily doses for the two groups were 30 and 20 mcg, respectively. A dose-response study (20 to 40 m cg/day) was carried out in group 5. Results: DDAVP spray therapy in primary monosymptomatic nocturnal enuresis was found to be resolutive in 70-75% of treated patients. No difference in response was found between the patients treated with the daily dose of 20 and those on 30 mcg. No important reacti ons were observed in patients treated with DDAVP spray at the different dai ly dose (20 to 30 mcg) or for different periods of time (up to 6 weeks). Co nclusions: DDAVP spray therapy at a dose of 20 mcg/day was effective in 70- 75% of primary monosymptomatic nocturnal enuretics. In non-responders the d aily dose of DDAVP should be increased to 30 to 40 mcg.