Aromatherapy Versus Diet
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: dietary recommendations, aroma therapy.
- Who it may be relevant to
- Registry conditions: Nocturnal Enuresis. Basic parameters: 5 years — 10 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Center list to be confirmed — check the primary protocol.
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Official title
Aromatherapy Versus Diet Management on Children with Primary Nocturnal Enuresis
Overview
Eligible children were randomly divided into 2 groups assigned to receive dietary recommendations (group A) or to receive herbal compounds (group B). Children were treated for a period of one week , then cross over the two groups is done
Interventions
- Behavioral dietary recommendations
. receive dietary recommendations or nonspecific dietary advices such as reducing fluid intake after 6 p.m. The list of dietary advices have been made reviewing literature and consisted in a list of recommended food, not recommended food at evening and not recommended food - Other aroma therapy
the case receive aroma therapy
Primary outcome measures
- number of wet days per week [Time frame: ; for baseline evaluation of number of wet days per week, if the number is less than 4\7 the child will be excluded from the study. Second week; group A receives dietary recommendations , group B receives herbal compounds]
Eligibility criteria
Inclusion criteria
- The participants age will be ranged from 5to 10 years.
- primary Nocturnal enuresis(NE) number of wet nights/week is more than 4\\7
Exclusion criteria
- secondary nocturnal enuresis to any neurological disorders , musculoskeletal problems, or congenital abnormalities
- the child receives any Pharmacological treatment to NE
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- Randomized
- Model
- Crossover
- Masking
- Single blind
- Primary purpose
- Treatment
Study locations
Center list to be confirmed — check the primary protocol.
Identifiers
NCT: NCT06853379 · aromatherapy versus diet