Dipartimento MeSVA
L’Aquila, Aq, 67100, Italy
NCT Number: NCT05848882
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:
* the efficacy of the two devices in the palatal expansion * the neuromuscolar effects developed on the stomatognatic system Participants will be instructed in the use and maintenance of the devices and will be checked every 15-30 days for one year.
Looking for future studies?
Notify Me9 year–15 year
All sexes
Interventional
Not applicable
L’Aquila, Aq, 67100, Italy
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
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
Removable device that embraces two dental archs
Time frame: 12 months
To compare the palatal first premolars width in three times
University of L'Aquila
Other
Comparison Between Removable Devices in Palatal Expansion: a Randomized Open Label Clinical Trial
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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