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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04518865
Other study ID # Herbst azhar
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date October 1, 2017
Est. completion date April 1, 2019

Study information

Verified date August 2020
Source Al-Azhar University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The study was directed to compare the treatment outcomes of subjects with Class II malocclusion who were treated with Herbst appliance before and after puberty.


Description:

Thirty-six Class II patients were randomly selected and divided into two groups based on their stage of skeletal maturation: pre-pubertal group (18 patients, mean age 9.15± 1.5 years) and post-pubertal group (18 patients, mean age 16.3 ± 1.0 years). All patients were treated with metallic splint supported Herbst IV appliance.

Pretreatment and post-Herbst IV treatment cone beam CT(CBCT) scans were obtained for both groups. Dentoskeletal and TMJ measurements made on the CBCT scans were analysed.


Recruitment information / eligibility

Status Completed
Enrollment 36
Est. completion date April 1, 2019
Est. primary completion date February 1, 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 8 Years to 17 Years
Eligibility Inclusion Criteria:

1. Skeletal Class II malocclusion with retrognathic mandible (ANB >5°, SNB<76°)

2. Normal growth pattern (SN/MP angle was in 25°- 35° range)

3. Unilateral or bilateral Class II molar relationship greater than or equal to one-half a cusp width.

4. Minimal or no crowding in the mandibular arch (0-5mm).

5. Average inclination or slight retroclination of the lower incisor.

6. An overjet greater than 5 mm.

Exclusion Criteria:

1. Skletal Class I

2. Craniofacial syndrome.

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Herbst appliance
The bottom line of the study is to investigate the changes after Herbst appliance treatment and relate it to the pubertal status of the skeletal class II patients using CBCT.

Locations

Country Name City State
Egypt Al-Azhar university Cairo

Sponsors (1)

Lead Sponsor Collaborator
Al-Azhar University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary Skeletal and dental changes The DICOM (Digital Imaging and Communications in Medicine) files from the pre and post CBCT scans were imported to Mimics software (Version 10.1, Materialise NV, Leuven, Belgium); and the cephalometric landmarks and planes were defined . Linear sagittal measurements of point A, point B, glenoid fossa, upper incisor, lower incisor, upper molars, and lower molars were recorded in relation to orbital perpendicular plane. 8 months
Secondary Condylar head position The Most middle-superior point of the mandibular condyle was determined in sagittal, axial and coronal views. In the sagittal slice of the middle condylar head, a line was drowned through the widest measurement of the condylar heads visible on the slice, from this line, three lines were raised crossing the glenoid fossa at 45°, 90°, and 135° . Four linear measurements representing the anterosuperior, superior, posterosuperior, and posterior distance were taken from the glenoid fossa wall to the surface of the condyle 8 months
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