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The Effect of Full Versus Partial Coverage Thermoformed Retainers in Dual Retention With a Lower Bonded Retainer, on Periodontal, Orthodontic, and Patient-Reported Outcomes

21 juillet 2026 mis à jour par: University of Malaya

The Effect of Full Versus Partial Coverage Thermoformed Retainers in Dual Retention With a Lower Bonded Retainer, on Periodontal, Orthodontic, and Patient-Reported Outcomes: A Randomised Controlled Trial

After braces are removed, teeth may move back toward their original positions. Retainers are used to help keep teeth straight after orthodontic treatment. This study compares two types of clear removable retainers used together with a fixed wire retainer behind the lower front teeth. One retainer covers the entire inner surface of the teeth (full coverage), while the other covers only part of the inner surface (partial coverage).

The purpose of this study is to find out whether the two retainer designs differ in their effects on gum health, comfort, retainer breakages, stability of the orthodontic correction, comfort, and compliance. The findings from this study may help orthodontists choose the most suitable retainer design for future patients.

Participants in this study will receive a fixed wire retainer on the lower front teeth and upper and lower clear removable retainers. They will be randomly assigned to receive either the full coverage or partial coverage lower retainer. Participants will attend follow-up visits at 1 month, 3 months, and 6 months after starting retainer wear. At these visits, the orthodontist will examine the teeth, gums, and retainers, and participants will complete a short questionnaire about their experience wearing the retainer.

This study excluded participants who are pregnant or breastfeeding within the first 6 months, have uncontrolled medical conditions or gum disease, smoke or vape, require a Hawley retainer instead of a clear retainer, or have missing front teeth or certain jaw conditions.

Participants may benefit from receiving retainers, oral hygiene care, and regular monitoring of their teeth and gum health at no additional cost. Participants will also receive an oral care kit during the debond appointment and at the 3-month and 6-month review visits.

Possible risks include breakage of the retainers, which may require repair or replacement, gum problems if oral hygiene is not maintained, and slight tooth movement despite retainer use. If gum problems develop, appropriate cleaning and referral for further treatment may be provided. Replacement retainers required during the study period will be provided free of charge.

Aperçu de l'étude

Description détaillée

Vivera retainers will be the only thermoformed retainers used throughout this study.

Type d'étude

Interventionnel

Inscription (Estimé)

42

Phase

  • N'est pas applicable

Contacts et emplacements

Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.

Coordonnées de l'étude

Lieux d'étude

    • Kuala Lumpur
      • Kuala Lumpur, Kuala Lumpur, Malaisie, 50603
        • Faculty of Dentistry, Universiti Malaya

Critères de participation

Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.

Critère d'éligibilité

Âges éligibles pour étudier

  • Adulte
  • Adulte plus âgé

Accepte les volontaires sains

Oui

La description

Inclusion Criteria:

  • Aged over 18 years.
  • Controlled systemic diseases and conditions.
  • Probing pocket depth ≤ 3 mm
  • Bleeding on probing < 10 per cent
  • Full mouth plaque scores of less than 20 per cent
  • Just completed active orthodontic treatment involving lower arch
  • Patient consent to dual retention in the lower arch

Exclusion Criteria:

  • Require a Hawley retainer in the lower arch.
  • Patients in retention phase requiring replacement of retainers
  • Uncontrolled systemic disease, including chronic or metabolic diseases.
  • Pregnant or lactating mothers within six months postpartum.
  • Taking medications that affect gingival health and architecture.
  • Have one or more missing anterior teeth.
  • Have congenital craniofacial deformities and syndromes, including cleft lip and/ or palate
  • Cigarette or vape smokers

Plan d'étude

Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.

Comment l'étude est-elle conçue ?

Détails de conception

  • Objectif principal: Traitement
  • Répartition: Randomisé
  • Modèle interventionnel: Affectation parallèle
  • Masquage: Aucun (étiquette ouverte)

Armes et Interventions

Groupe de participants / Bras
Intervention / Traitement
Comparateur actif: Full coverage clear retainer
A removable lower retainer covers the entire inside surface of lower teeth including the fixed bonded retainer
A removable lower retainer (Vivera retainer) with full coverage design which covers the entire inside surface of lower teeth including the fixed bonded retainer
Comparateur actif: Partial coverage clear retainer
A removable lower retainer covers part of inside surface of lower teeth excluding the fixed bonded retainer
A removable lower retainer (Vivera retainer) with partial coverage design which covers part of the inside surface of lower teeth excluding the fixed bonded retainer

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
Full mouth plaque score
Délai: baseline, 1 month, 3 months and 6 months

To evaluate full mouth plaque score associated with clear retainers with partial or full coverage designs when used in conjunction with fixed bonded retainers in the lower arch.

Scale title: Full mouth plaque score Minimum value: 0% Maximum value: 100% Higher score means indicate worse plaque accumulation and poorer oral hygiene. (worse outcome)

baseline, 1 month, 3 months and 6 months
Full mouth bleeding on probing score
Délai: Baseline, 1 month, 3 months and 6 months

To evaluate full mouth bleeding on probing score associated with clear retainers with partial or full coverage designs when used in conjunction with fixed bonded retainers in the lower arch.

Scale title: Full mouth bleeding on probing score Minimum value: 0% Maximum value: 100% Higher score means indicate worse periodontal health (worse outcome)

Baseline, 1 month, 3 months and 6 months
Periodontal probing depth of lower anterior teeth
Délai: baseline, 1 month, 3 months and 6 months

To evaluate periodontal probing depth of lower anterior teeth associated with clear retainers with partial or full coverage designs when used in conjunction with fixed bonded retainers in the lower arch

Scale title: Periodontal probing depth Minimum value: 0mm Maximum value: No fixed upper limit Higher score means indicate worse periodontal health (worse outcome)

baseline, 1 month, 3 months and 6 months
Gingival recession on lower anterior teeth
Délai: Baseline, 1 month, 3 months and 6 months

To evaluate gingival recession on lower anterior teeth associated with clear retainers with partial or full coverage designs when used in conjunction with fixed bonded retainers in the lower arch

Scale title: Gingival recession Minimum value: 0mm Maximum value: No fixed upper limit Higher score means indicate worse periodontal health (worse outcome)

Baseline, 1 month, 3 months and 6 months
Integrity of clear retainer
Délai: 3 months and 6 months
To evaluate the incidence of clear retainer breakages associated with partial or full coverage designs when used in combination with fixed bonded retainers in the lower arch
3 months and 6 months
Breakages of fixed bonded retainers
Délai: 1 month, 3 months, 6 months
To evaluate the incidence of breakages involving bonded wire or adhesive resin of fixed bonded retainers when used in combination with clear retainers in either partial or full coverage designs in the lower arch.
1 month, 3 months, 6 months

Mesures de résultats secondaires

Mesure des résultats
Description de la mesure
Délai
Stability of lower anterior teeth
Délai: Baseline, 3 months, 6 months

To evaluate the stability of lower anterior teeth (using Little's Irregularity Index) associated with partial and full coverage designs of clear retainers when used in conjunction with fixed bonded retainers.

Scale title: Little's Irregularity Index Minimum value: 0mm Maximum value: No fixed upper limit Higher scores indicate greater relapse and worse alignment. (worse outcome)

Baseline, 3 months, 6 months
Quality of Life in Patients Wearing Orthodontic Retainers
Délai: 3 months and 6 months
To evaluate the patient's quality of life associated with partial or full coverage designs of clear retainers when used in conjunction with fixed bonded retainers. Quality of life assessed using the Quality of Life in Patients Wearing Orthodontic Retainers questionnaire. Total scores range from 0 score to 56 score, with higher scores indicating poorer quality of life related to retainer wear.
3 months and 6 months
Patient's compliance
Délai: 3 months and 6 months
Patient compliance associated with partial or full coverage clear retainers used in conjunction with fixed bonded retainers will be evaluated using Part B, Questions 1 and 2 of the Quality of Life in Patients Wearing Orthodontic Retainers questionnaire. Compliance will be reported as "yes" or "no." For non-compliance responses, reasons for non-compliance will also be recorded, with multiple responses permitted.
3 months and 6 months

Collaborateurs et enquêteurs

C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.

Dates d'enregistrement des études

Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.

Dates principales de l'étude

Début de l'étude (Estimé)

1 juillet 2026

Achèvement primaire (Estimé)

30 juin 2027

Achèvement de l'étude (Estimé)

30 septembre 2027

Dates d'inscription aux études

Première soumission

12 mai 2026

Première soumission répondant aux critères de contrôle qualité

21 juin 2026

Première publication (Réel)

25 juin 2026

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

23 juillet 2026

Dernière mise à jour soumise répondant aux critères de contrôle qualité

21 juillet 2026

Dernière vérification

1 mai 2026

Plus d'information

Termes liés à cette étude

Autres numéros d'identification d'étude

  • DF CD2609/0046 (P)

Plan pour les données individuelles des participants (IPD)

Prévoyez-vous de partager les données individuelles des participants (DPI) ?

NON

Informations sur les médicaments et les dispositifs, documents d'étude

Étudie un produit pharmaceutique réglementé par la FDA américaine

Non

Étudie un produit d'appareil réglementé par la FDA américaine

Non

Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .

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