Clinical and Radiographic Evaluation of Different Thickness of Vacuum Formed Retainer (Essix Retainer) During Retention Phase After Orthodontic Treatment
NCT ID: NCT04149366
Last Updated: 2019-11-04
Study Results
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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UNKNOWN
40 participants
OBSERVATIONAL
2019-10-29
2020-10-25
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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group 1 (Wrapround retainer)
Retainer
Orthodontic retainer
Group 2 (Essix retainer 1mm)
No interventions assigned to this group
Group 3 (Essix retainer 1.5 mm)
No interventions assigned to this group
Group 3 (Essix retainer 2mm)
No interventions assigned to this group
Interventions
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Retainer
Orthodontic retainer
Eligibility Criteria
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Inclusion Criteria
* patients indicated for removable retainer
Exclusion Criteria
* chronic medication uptake
* bad oral hygiene pathological conditions of temporomandibular joint
15 Years
35 Years
ALL
No
Sponsors
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Minia University
OTHER
Responsible Party
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Mostafa Ahmed
assistant lecturer
Other Identifiers
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295
Identifier Type: -
Identifier Source: org_study_id
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