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Clinical Trials/NCT05626335
NCT05626335CompletedNot Applicable

Does Double (Fixed and Removable Orthodontic Retention) With Regular Monitoring Prevent Undesired Tooth Movement?

Pomeranian Medical University Szczecin1 site in 1 country100 target enrollmentStarted: January 1, 2021Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
100
Locations
1
Primary Endpoint
Tooth displacement in mm

Study Overview

Brief Summary

The goal of observational study is to learn about the stability of orthodontic treatment results in orthodontic patients during retention phase of treatment.

Detailed Description

The aim of the present study was to three-dimensionally analyze tooth movement in retention phase of treatment and wherever double effectively retention prevents it.

Study Design

Study Type
Observational
Observational Model
Case Only
Time Perspective
Prospective

Eligibility Criteria

Ages
18 Years to 65 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Non-extraction treatment
  • No hypodontia
  • Normal occlusion after treatment (Class I occlusion), perfect alignment
  • Normal overjet and overbite
  • Double retention including fixed retainer bonded from canine to canine in both dental arches and thermally formed removable splint

Exclusion Criteria

  • Fixed orthodontic treatment in one dental arch
  • Extraction cases
  • Patient treated with orthognathic surgery
  • Imperfect treatment result due to treatment cessation on patients demand or health issues
  • Craniofacial disorders

Outcomes

Primary Outcomes

Tooth displacement in mm

Time Frame: Six months after debonding

Measurement obtained by comparing superimposed scans

Secondary Outcomes

  • Compliance rate(Six months of observation)
  • Failure rate(Six months of observation)

Investigators

Sponsor
Pomeranian Medical University Szczecin
Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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