Mandibular Advancement Planning Based on Clinical Overjet

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age6-50
SponsorIRCCS Ospedale San Raffaele

About this trial

This Prospective study aims to simulate the maximum mandibular advancement in class II patients treated by Herbst MTH Appliance on the base on clinical overjet.

Initial intraoral scans will be uploaded in Suresmile software, the upper incisors will be virtually aligned and the mandible will be advancement until an anterior occlusal contact will be reached. This virtual advancement will be compared to the real advancement obtained at the end of the Herbst phase.

This protocol will be applied to two groups: one with traditional dental occlusion, the second one with Skeletal anchorage reinforcement and elastic chains

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

ANB>=4°

Overjet >=4 mm

Class II malocclusion ( bilateral class II molar relation, at least half a cusp)

Disqualifiers

tooth agenesis

poor oral hygiene

previous orthodontic treatments

systemic disease or bone pathology

Trial design

Design model

Parallel

Treatments tested in this trial

  • mandibular advancement with acrylic splint Herbst Appliance

    Procedure/Surgery

    Mandibular advancement with acrylic splint Herbst Appliance

Treatment groups

50 Participants
are divided into 2 treatment groups
Group A: traditional anchorageActive comparator 1 intervention
Group B: skeletal anchorageExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Planned mandibular advancement (mm)

The "planned mandibular advancement" will be evaluated on the STL of the arches by simulating a sagittal mandibular advancement , until an anterior occlusal contact will be reached

Time frame
1 year

Secondary outcomes

1

Obtained mandibular advancement (mm)

The obtained mandibular advancement will be evaluated comparing the Sagittal position of the Pogonion (according to cephalometric pancherz's analysis) on the lateral ceph before and after the treatment

Time frame
1 year

Other outcomes

Sponsors and contacts

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This trial is not recruiting at the moment. You can still explore other options: