Assessment of Dentoskeletal Changes After Treatment of Skeletal classII by Twinblock Versus Monoblock Appliances

NCT ID: NCT07277543

Last Updated: 2025-12-11

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

18 participants

Study Classification

INTERVENTIONAL

Study Start Date

2023-10-25

Study Completion Date

2025-09-25

Brief Summary

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Assessment of dentoskeletal changes after treatment of skeletal classII growing patient by twin block versus mono block ,clinical trial stuy

Detailed Description

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Group(A):patients will be treated with twinbLock Group(B):patients will be treated with monobLock

Conditions

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Dentoskeletal Changes in Skeletal classII

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

CROSSOVER

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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treatment of skeletal classII by twin block

growing patient wearing twin block appliance15 hrs/day

Group Type EXPERIMENTAL

wearing of twinblock after bite correction

Intervention Type DEVICE

bite registration at edge to edge position ,twin block wearing 15hrs/day

treatment of skeletal classII by monoblock

growing patients wearing monoblck appliance15hrs/day

Group Type EXPERIMENTAL

wearing of monoblock after bite correction

Intervention Type DEVICE

bite registration at edge to edge position ,mono block wearing 15hrs/day

Interventions

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wearing of twinblock after bite correction

bite registration at edge to edge position ,twin block wearing 15hrs/day

Intervention Type DEVICE

wearing of monoblock after bite correction

bite registration at edge to edge position ,mono block wearing 15hrs/day

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

* Female patients to avoid any sexual dimorphism which may affect the comparison.
* Skeletal Class II (ANB° \> 5°) with normal maxilla (SNA° = 82° ±4°) and retrognathic mandible (SNB° \< 87°).
* Age range from 9 to 12 years.

Exclusion Criteria

* Previous history of orthodontic treatment.
* Congenitally missing or extracted permanent teeth.
* Posterior cross bites or severe maxillary transverse deficiency.
* Severe facial asymmetry determined by clinical or radiographic examination.
* Poor oral hygiene.
* Systemic diseases that may affect the treatment results.
Minimum Eligible Age

9 Years

Maximum Eligible Age

12 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No

Sponsors

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Faculty of Dental Medicine for Girls

OTHER_GOV

Sponsor Role lead

Responsible Party

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Shimaa Nasr

principle investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Maha Mostafa Mohammed, Ass.Professor

Role: PRINCIPAL_INVESTIGATOR

Ass.Professor of Orthodontics

Locations

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Shimaa Nasr

Cairo, , Egypt

Site Status

Countries

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Egypt

References

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Sakuno AC, da Rosa APB, Maeda FA, Trivino T, Carvalho PEG, Torres FC. Tomographic evaluation of dentoskeletal changes due to the treatment of class II malocclusion with Forsus appliance. J Oral Biol Craniofac Res. 2019 Jul-Sep;9(3):277-279. doi: 10.1016/j.jobcr.2019.06.005. Epub 2019 Jun 5.

Reference Type RESULT
PMID: 31289716 (View on PubMed)

Related Links

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https://pubmed.ncbi.nlm.nih.gov/31289716/

evaluation of dentoskeletal changes due to the treatment of class II malocclusion

Other Identifiers

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ORTHO-108-2-H

Identifier Type: -

Identifier Source: org_study_id

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