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Clinical Trials in Italy / NCT06653075
Starting soon Not applicable

Mandibular Advancement Planning Based on Clinical Overjet

NCT06653075 · tracked via the Priya Life Science Italy tracker
Sponsor
IRCCS Ospedale San Raffaele
Phase
Not applicable
Started
2024-10-30
Last updated
2024-10-23

Condition(s) studied

OverjetClass II Division 1 Malocclusion

Investigational drug(s) / intervention(s)

mandibular advancement with acrylic splint Herbst Appliance

mandibular advancement with acrylic splint Herbst Appliance: Mandibular advancement with acrylic splint Herbst Appliance

Study summary

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

Sex
ALL
Min age
6 Years
Max age
50 Years
Healthy volunteers
Accepted
Inclusion Criteria: * ANB\>=4° * Overjet \>=4 mm * Class II malocclusion ( bilateral class II molar relation, at least half a cusp) Exclusion Criteria: * tooth agenesis * poor oral hygiene * previous orthodontic treatments * systemic disease or bone pathology

Primary outcome measure(s)

  • Planned mandibular advancement (mm) — 1 year
    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

Trial sites (1)

FacilityCityRegionStatus
Vita-Salute San Raffaele University Milan Italy

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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 NCT06653075 on ClinicalTrials.gov ↗ ← All trials in Italy