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Clinical Trials in Italy / NCT06187337
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Interceptive Maxillary Expansion to Relief Anterior Crowding in the Mixed Dentition

NCT06187337 · tracked via the Priya Life Science Italy tracker
Phase
Not applicable
Started
2021-12-20
Last updated
2025-07-18

Condition(s) studied

Crowding of Anterior Maxillary TeethOrthodontics, InterceptiveOrthodontics, Corrective, Palatal Expansion Technique

Investigational drug(s) / intervention(s)

Maxillary expansion device

Maxillary expansion device: The maxillary expansion device is a orthodontic appliance that is used to expand the maxilla in children.

Study summary

The goal of this clinical trial is to compare if it is better to treat severe anterior crowding in the early mixed dentition then later in the permanent dentition in children with anterior crowding of the upper teeth. The main questions this trial aims to answer are:

* If there is a difference in the degree of anterior crowding between the experimental group and the control group after a five year follow-up period.
* If there is a difference between the experimental group and the control group in regard to oral health related quality of life.
* If there is spontaneous transversal adaption of the lower dental arch to upper dental arch after maxillary expansion and compare this to the control group.
* If early maxillary expansion is more cost-effective than treatment in the permanent dentition.

To be eligible for this trial the subject must be children between six and nine years old at the time for inclusion. The children must have crowding of the upper front teeth of six millimeters or more and the lateral incisors should not have erupted or just erupted through the gingiva.

Subjects randomized to the experimental group will get an expansion treatment in the upper jaw with rapid maxillary expansion device to gain enough space for the lateral incisors to erupt. All subjects, also the subjects randomized to the control group, are followed until all permanent teeth have erupted.

At the end of the follow-up period all subjects fill out a questionnaire to evaluate their oral health related quality of life.

Researchers will then compare the subjects in both groups to evaluate if there is a difference in anterior crowding after the follow-up period. Differences in cost-effectiveness, morphological changes and the subjects oral health related quality of life will also be evaluated.

Eligibility

Sex
ALL
Min age
6 Years
Max age
16 Years
Healthy volunteers
No
Inclusion Criteria: * Healthy subjects without sucking habits * Permanent maxillary central incisors and first permanent molars fully erupted. DS1M1. * No severe crowding or protrusion in the lower arch considering the Leeway space and normal development of the arch. * Permanent first molar in normal transversal relation. * Crowding of the maxillary incisors with the lateral incisor just erupting ectopically or not yet emerged through the gingiva. * Crowding greater than or equal to 6 millimeters between the upper deciduous canines. Exclusion Criteria: * Skeletal asymmetries, anomalies and syndromes. * Previous orthodontic treatment

Primary outcome measure(s)

Trial sites (4)

FacilityCityRegionStatus
Postgraduate School of Orthodontics, University of L'Aquila Coppito Italy Recruiting
Universita Degli Studi Di Milano Milan Italy Recruiting
The Institute for Postgraduate Dental Education in Jönköping Jönköping Sweden Recruiting
Emil Östlund Örebro Sweden Recruiting

More Region Örebro County trials in Italy

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06187337 on ClinicalTrials.gov ↗ ← All trials in Italy