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Rapid maxillary expansion in children with nocturnal enuresis: A randomized placebo-controlled trial
Insights
Rapid maxillary expansion (RME) modestly improves nocturnal enuresis (NE) in children resistant to other treatments. A wide maxilla and large voiding volume predict successful outcomes, suggesting RME is a viable therapy beyond placebo effects.
Area of Science:
- Pediatric Urology
- Orthodontics
- Sleep Medicine
Background:
- Nocturnal enuresis (NE) is a common condition in children, often requiring multidisciplinary treatment approaches.
- Therapy-resistant NE presents a significant challenge, necessitating exploration of novel treatment modalities.
- Rapid maxillary expansion (RME) is an orthodontic procedure with potential, yet unproven, benefits for NE.
Purpose of the Study:
- To evaluate the efficacy of RME as a treatment for therapy-resistant NE in children.
- To determine if any observed treatment effects are attributable to a placebo response.
- To identify prognostic factors associated with a positive response to RME treatment for NE.
Main Methods:
- A randomized controlled trial involving 38 children with therapy-resistant NE.
- Intervention group received RME; placebo group received a sham appliance followed by RME.
- Baseline assessments included medical history, voided volumes, and nocturnal urine production.
Main Results:
- RME treatment resulted in a statistically significant reduction in wet nights (P < .001).
- No significant reduction in wet nights was observed following placebo treatment (P < .40).
- Over 35% of patients experienced a >50% reduction in enuresis frequency; wide maxilla and large voiding volume were positive predictors.
Conclusions:
- RME demonstrates a modest but significant effect in treating children with therapy-resistant NE.
- The positive outcomes are unlikely to be solely due to a placebo effect of the appliance.
- Maxillary width and baseline voiding volume are identified as key predictors for successful RME treatment in NE.
Objective:
To investigate whether rapid maxillary expansion (RME) is a useful treatment method for nocturnal enuresis (NE) and whether the treatment effect is due to placebo. The study also aimed to identify prognostic variables in patients responding to treatment.
Materials And Methods:
Thirty-eight children with therapy-resistant NE were recruited and randomized into two groups: the intervention group or placebo group. Both groups were treated with RME, but the placebo group received treatment with a sham appliance for 2 weeks before having the actual treatment. A medical history focused on micturition habits, previous treatment, heredity, and sleep disorders was taken. Daytime voided volumes and nocturnal urine production during wet nights were recorded before the intervention.
Results:
Of the 38 patients recruited, two dropped out as one patient was unable to take dental impressions and one refused to have the appliance fitted. There was a statistically significant reduction of wet nights after the RME treatment (P < .001). No significant reduction was found after the placebo treatment (P < .40). Eleven patients (35%) had their enuresis frequency reduced by >50%. Large voiding volume and a wide maxilla at baseline had a strong association with positive treatment outcome.
Conclusions:
RME has a modest effect on children with therapy-resistant NE. The treatment outcome does not seem to be due to a placebo effect of the appliance. A wide maxillary width and large voiding volume at baseline seem to be positive predictors regarding response to treatment.
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