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About
The goal of this clinical trial si to compare two removable devices used to treat the transversal discrepancies in growing patients.
The main questions it aims to answer are:
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Inclusion criteria
skeletal class I relationship, molar class I relationship; complete eruption of upper first premolars ; presence of unilateral or bilateral cross bite (falling within grade 3 IOTN index)
Exclusion criteria
IOTN index >4; presence of temporomandibular disorders, epilepsy, systemic diseases, periodontal disease, absence of written informed consent signed by parents/legal guardians
Primary purpose
Allocation
Interventional model
Masking
70 participants in 2 patient groups
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Data sourced from clinicaltrials.gov
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