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Clinical and Radiographic Evaluation of Different Thickness of Vacuum Formed Retainer (Essix Retainer) During Retention Phase After Orthodontic Treatment

M

Minia University

Status

Unknown

Conditions

Temporomandibular Joint Disorders After Using Essix Retainer

Treatments

Device: Retainer

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

vacuum formed retainer act as bite raiser that increase vertical dimension which may affect Tempromandibular joint and aim of this study is to perform clinical and radiographic evaluation of different thickness of vacuum formed retainer (Essix retainer) during retention phase after orthodontic treatment

Enrollment

40 estimated patients

Sex

All

Ages

15 to 35 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • patients finished fixed orthodontic treatment with no signs or symptoms of temporomandibular joint disorders
  • patients indicated for removable retainer

Exclusion criteria

  • any systemic disease
  • chronic medication uptake
  • bad oral hygiene pathological conditions of temporomandibular joint

Trial design

40 participants in 4 patient groups

group 1 (Wrapround retainer)
Treatment:
Device: Retainer
Group 2 (Essix retainer 1mm)
Group 3 (Essix retainer 1.5 mm)
Group 3 (Essix retainer 2mm)

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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