orthoretenti: Efficacy and Cost-effectiveness of Orthodontic Retention Protocols

Sponsor
Poliklinika Orthonova (Other)
Overall Status
Recruiting
CT.gov ID
NCT05121220
Collaborator
University of Zagreb School of Dental Medicine, Zagreb, Croatia (Other), University of Rijeka Faculty of Dental Medicine, Rijeka, Croatia (Other)
152
1
3
36
4.2

Study Details

Study Description

Brief Summary

Objective is to assess changes of dentition and periodontium, and hygiene in retention after the end of the active phase of orthodontic treatment, and relationship with gender, type of retention appliance, pre-therapeutic condition of dentition and duration of active phase of treatment.

Condition or Disease Intervention/Treatment Phase
  • Device: fixed retainer
  • Device: removable retainer
N/A

Detailed Description

A total of 152 subjects will be recruited and randomly assigned into three groups. First group will have a square 8-stranded 0.673x0.268 mm retainer wire bonded in mandibular teeth after completing the active phase of comprehensive orthodontic treatment with fixed appliances. Retainer will be bonded on lingual site canine to canine on each tooth. Second group will have a round 6-stranded 0.40 mm retainer in mandible. Third group will be without fixed retainer, only with thermoplastic vacuum-formed removable Essix retainer in mandible.

Subjects will be examined before orthodontic treatment (T0), upon completion of treatment (T1), six months in retention (T2), two years (T3) and three years in retention (T4). Changes in intercanine width, relapse (unexpected tooth movements), retainer failure, accumulation of biofilm, calculus and gingivitis will be assessed.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
152 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Investigator)
Primary Purpose:
Prevention
Official Title:
Efficacy and Cost-effectiveness of Orthodontic Retention Protocols
Actual Study Start Date :
Nov 15, 2020
Anticipated Primary Completion Date :
Nov 15, 2022
Anticipated Study Completion Date :
Nov 15, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: fixed mandibular lingual rectangular retainer 0.673 x 0.268 mm

0.673 x 0.268 mm 8-stranded wire Bond A Braid (Reliance Orthodontic Products, USA) will be bonded in mandible canine to canine on each tooth using Filtek flowable composite (Ivoclar Vivadent, Lichtenstein) and Multilink adhesive (3M, USA).

Device: fixed retainer
bonded lingual mandibular fixed retainer on frontal teeth 33-43

Experimental: fixed mandibular lingual round retainer 0.40 mm

0.40 mm round 6-stranded wire (Forestadent, Germany) will be bonded on 6 mandibular frontal teeth, canine to canine on each tooth using Filtek flowable composite (Ivoclar Vivadent, Lichtenstein) and Multilink adhesive (3M, USA).

Device: fixed retainer
bonded lingual mandibular fixed retainer on frontal teeth 33-43

Active Comparator: removable mandibular retainer

Group without fixed retainer will be wearing removable thermoplastic vacuum-formed Essix retainer

Device: removable retainer
thermoplastic vacuum-formed removable mandibular retainer

Outcome Measures

Primary Outcome Measures

  1. severity of relapse (unexpected tooth movement in mandibular frontal area) at 1 year [1 year]

    the unabbreviated scale title: Little Irregularity Index (used to measure the crowding)- numerical rating scale in millimeters the minimum and maximum values: 0,10 higher scores mean a worse outcome lower scores mean a better outcome

  2. severity of relapse (unexpected tooth movement in mandibular frontal area) at 2 years [2 years]

    the unabbreviated scale title: Little Irregularity Index (used to measure the crowding)- numerical rating scale in millimeters the minimum and maximum values: 0,10 higher scores mean a worse outcome lower scores mean a better outcome

  3. severity of relapse (unexpected tooth movement in mandibular frontal area) at 3 years [3 years]

    the unabbreviated scale title: Little Irregularity Index (used to measure the crowding)- numerical rating scale in millimeters the minimum and maximum values: 0,10 higher scores mean a worse outcome lower scores mean a better outcome

  4. incidence of retainer failure (debonding, breakage) at 2 years [2 years]

    percentage of cases with at least one fixed retainer failure, the minimum and maximum values 0%,100% higher scores mean a worse outcome, lower scores mean a better result

  5. incidence of retainer failure (debonding, breakage) at 3 years [3 years]

    percentage of cases with at least one fixed retainer failure, the minimum and maximum values 0%,100% higher scores mean a worse outcome, lower scores mean a better result

  6. extent of biofilm accumulation at 2 years [2 years]

    the unabbreviated scale title: Silness and Loe Plaque Index-ratio of measuring sites in mandibular central sextant; the minimum and maximum values 0%,100%, higher scores mean a worse outcome, lower scores mean a better result

  7. extent of biofilm accumulation at 3 years [3 years]

    the unabbreviated scale title: Silness and Loe Plaque Index-ratio of measuring sites in mandibular central sextant; the minimum and maximum values 0%,100%, higher scores mean a worse outcome, lower scores mean a better result

Secondary Outcome Measures

  1. incidence of intercanine width change [3 years]

    percentage of cases with intercanine width change, the minimum and maximum values 0%,100% higher scores mean a worse outcome, lower scores mean a better result

  2. changes of intercanine width [2 years, 3 years]

    the unabbreviated scale title: intercanine width change in millimeters, the minimum and maximum values 0,5, higher scores mean a worse outcome, lower result mean a better outcome

  3. extent of calculus accumulation at 2 years [2 years]

    the unabbreviated scale title: Calculus Surface Index (CSI)-ratio of measuring sites in mandibular central sextant; the minimum and maximum values 0%,100%, higher scores mean a worse outcome, lower scores mean a better outcome

  4. extent of calculus accumulation at 3 years [3 years]

    the unabbreviated scale title: Calculus Surface Index (CSI)-ratio of measuring sites in mandibular central sextant; the minimum and maximum values 0%,100%, higher scores mean a worse outcome, lower scores mean a better outcome

Other Outcome Measures

  1. incidence of relapse at 2 years [2 years]

    the unabbreviated scale title: percentage of relapsed cases; the minimum and maximum values 0%,100%, higher scores mean a worse outcome, lower scores mean a better outcome

  2. incidence of relapse at 3 years [3 years]

    the unabbreviated scale title: percentage of relapsed cases; the minimum and maximum values 0%,100%, higher scores mean a worse outcome, lower scores mean a better outcome

  3. extent of gingivitis at 2 years [2 years]

    the unabbreviated scale title: Bleeding on probing (BOP)-ratio of measuring sites in mandibular central sextant; the minimum and maximum values 0%,100%, higher scores mean a worse outcome, lower scores mean a better result

  4. extent of gingivitis at 3 years [3 years]

    the unabbreviated scale title: Bleeding on probing (BOP)-ratio of measuring sites in mandibular central sextant; the minimum and maximum values 0%,100%, higher scores mean a worse outcome, lower scores mean a better result

  5. duration of orthodontic treatment in months [1 year]

    the unabbreviated scale title: numerical rating scale the minimum and maximum values: 0,30

  6. satisfaction with stability of results in retention period [3 years]

    Participant's satisfaction with stability of results as assessed using a 5-point Likert scale. Scores range from "very unsatisfied" (1) to "very satisfied" (5). Higher scores mean a better outcome, lower scores mean a worse outcome

  7. costs total [3 years]

    calculation of costs of retention: failures and new retainers in euros

  8. loss of productivity [3 years]

    the unabbreviated scale title: number of check-ups in retention period; the minimum and maximum values 0,10; higher scores mean a worse outcome, lower scores mean a better result the minimum and maximum values: 0,30

Eligibility Criteria

Criteria

Ages Eligible for Study:
11 Years to 18 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes

Inclusion Criteria: finished orthodontic treatment, participants must have all permanent teeth Exclusion Criteria: hypodontia, missing teeth

Contacts and Locations

Locations

Site City State Country Postal Code
1 Poliklinika Orthonova Zagreb Croatia 10000

Sponsors and Collaborators

  • Poliklinika Orthonova
  • University of Zagreb School of Dental Medicine, Zagreb, Croatia
  • University of Rijeka Faculty of Dental Medicine, Rijeka, Croatia

Investigators

  • Principal Investigator: Silvija Kanižaj Ugrin, DDM, Poliklinika Orthonova

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
silvija kanižaj ugrin, Dentist, Orthodontic specialist, Poliklinika Orthonova
ClinicalTrials.gov Identifier:
NCT05121220
Other Study ID Numbers:
  • 66771011
First Posted:
Nov 16, 2021
Last Update Posted:
May 9, 2022
Last Verified:
May 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by silvija kanižaj ugrin, Dentist, Orthodontic specialist, Poliklinika Orthonova
Additional relevant MeSH terms:

Study Results

No Results Posted as of May 9, 2022