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Comparison of AMCOP Bioactivator and High-pull Headgear in Treating Skeletal Class II Hyperdivergent Pediatric Patients

U

University of Pavia

Status

Completed

Conditions

Skeletal Malocclusion

Treatments

Device: High-pull headgear
Device: AMCOP group

Study type

Observational

Funder types

Other

Identifiers

NCT06281613
2024-AMCOPTEO

Details and patient eligibility

About

The aim of the present study was to retrospectively compare the clinical use of high-pull headgear versus AMCOP bioactivators for hyperdivergent pediatric patients.

Cephalometric radiographs from pediatric patients treated at the Unit of Orthodontics and Pediatric Dentistry, Section of Dentistry, Department of Clinical, Surgical, Diagnostic and Pediatric Sciences, University of Pavia, Pavia, Italy and at the private practice of Dr. Cardarelli, Isernia, Italy will be collected.

Cephalometric tracing from Giannì analysis will be performed at the baseline (T0) and after 18 months of treatment (T1).

Full description

The aim of the present study was to retrospectively compare the clinical use of high-pull headgear versus AMCOP bioactivators for hyperdivergent pediatric patients.

Cephalometric radiographs from pediatric patients treated at the Unit of Orthodontics and Pediatric Dentistry, Section of Dentistry, Department of Clinical, Surgical, Diagnostic and Pediatric Sciences, University of Pavia, Pavia, Italy and at the private practice of Dr. Cardarelli, Isernia, Italy will be collected.

Cephalometric tracing from Giannì analysis will be performed at the baseline (T0) and after 18 months of treatment (T1).

Enrollment

40 patients

Sex

All

Ages

7 to 11 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • mixed or permanent dentition
  • skeletal class II malocclusion diagnosed with ANB angle > 4° from cephalometric radiograph
  • skeletal hyperdivergency calculated from AnsPns^GoGn angle > 25°, and at least S-Ar^Go > 149° or Ar-Go^Gn > 137°

Exclusion criteria

  • lack of compliance in the use of the orthodontic appliance
  • syndromic patients, cleft lip or cleft palate, severe malformations and asymmetries of the jaws.

Trial design

40 participants in 2 patient groups

Case group
Treatment:
Device: AMCOP group
Control Headgear
Treatment:
Device: High-pull headgear

Trial contacts and locations

1

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Central trial contact

Andrea Scribante, DDS, PhD, Mac

Data sourced from clinicaltrials.gov

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