Zirconia and Bioflx Crowns for Primary Anterior Teeth
Clinical Outcomes of Prefabricated Zirconia and Bioflx Crowns for Restoring Primary Maxillary Anterior Teeth: A Randomized Controlled Trial
This parallel-group randomized controlled trial will compare the clinical performance of prefabricated zirconia and Bioflx crowns for restoring primary maxillary anterior teeth in children aged 3 to 5 years. Eligible participants will be randomly assigned in a 1:1 ratio to receive either a zirconia crown or a Bioflx crown.
Clinical outcomes will be assessed at 3, 6, and 12 months after crown placement. Evaluations will include gingival health, plaque accumulation, wear of the opposing tooth, crown retention, and clinical symptoms of the treated tooth. Parent satisfaction with the esthetic outcome will also be evaluated.
The study aims to provide comparative clinical evidence on the effectiveness of zirconia and Bioflx crowns for restoration of primary maxillary anterior teeth.
Studieöversikt
Status
Betingelser
Intervention / Behandling
Detaljerad beskrivning
Primary maxillary anterior teeth are important for esthetics, speech, mastication, and maintenance of normal oral function in young children. Extensive caries and hypomineralization may result in substantial loss of tooth structure and require full-coverage restoration. Prefabricated zirconia and Bioflx crowns are esthetic restorative options; however, comparative clinical evidence for their use in primary maxillary anterior teeth remains limited.
This study is a parallel-group randomized controlled clinical trial conducted in children aged 3 to 5 years who require full-coverage restoration of primary maxillary anterior teeth. Eligible participants must have an opposing tooth and at least two carious surfaces on the target tooth, caries involving the incisal edge, or discoloration associated with hypomineralization. Children with acute systemic disease, allergy to the luting cement, pulp exposure before treatment, inadequate remaining tooth structure, severe bruxism or deep bite, advanced root resorption, previous trauma affecting the target tooth, or other predefined exclusion criteria will not be enrolled.
A minimum of 120 teeth will be included. Randomization will be performed at the participant level using a computer-generated variable block sequence with a 1:1 allocation ratio. Allocation concealment will be maintained using sequentially numbered opaque sealed envelopes.
Participants will receive either prefabricated zirconia crowns or prefabricated Bioflx crowns. Clinical and radiographic examinations will be completed before treatment. Crown preparation and cementation procedures will be standardized, and Fuji IX Extra glass ionomer cement will be used for crown placement.
The primary outcome will be gingival health at 6 months after crown placement. Secondary outcomes will include plaque accumulation, wear of opposing teeth, crown retention, clinical symptoms of crowned teeth, and parent satisfaction with crown esthetics. Follow-up assessments will be performed at 3, 6, and 12 months. Statistical analyses will account for clustering when more than one tooth is included from the same participant.
Studietyp
Inskrivning (Beräknad)
Fas
- Inte tillämpbar
Kontakter och platser
Studieorter
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Huế, Vietnam, 530000
- Faculty of Odonto-Stomatology, University of Medicine and Pharmacy, Hue University
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Deltagandekriterier
Urvalskriterier
Åldrar som är berättigade till studier
- Barn
Tar emot friska volontärer
Beskrivning
Inclusion Criteria:
- Children aged 3 to 5 years.
- Children requiring full-coverage restoration of one or more primary maxillary anterior teeth.
- Presence of an opposing tooth.
- Target tooth with at least two carious surfaces, caries involving the incisal edge, or discoloration associated with hypomineralization.
- Written informed consent from a parent or legal guardian and willingness to comply with treatment and follow-up visits.
Exclusion Criteria:
- Allergy to Fuji IX Extra glass ionomer cement.
- Acute systemic disease.
- Crowded teeth affecting crown placement.
- Pulp exposure before treatment.
- Inadequate remaining clinical crown structure after tooth preparation.
- Absence of an opposing tooth.
- Bruxism or deep bite.
- Tooth close to exfoliation or root resorption exceeding one-half of the root length.
- Caries limited to a single surface without proximal involvement.
- History of trauma affecting the target tooth.
Studieplan
Hur är studien utformad?
Designdetaljer
- Primärt syfte: Behandling
- Tilldelning: Randomiserad
- Interventionsmodell: Parallellt uppdrag
- Maskning: Ingen (Open Label)
Vapen och interventioner
Deltagargrupp / Arm |
Intervention / Behandling |
|---|---|
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Aktiv komparator: Zirconia
Participants receive prefabricated zirconia crowns for restoration of indicated primary maxillary anterior teeth.
Teeth are prepared using a standardized clinical protocol, and crowns are cemented with Fuji IX Extra glass ionomer cement.
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Prefabricated zirconia crowns manufactured by Shinhung, Republic of Korea, will be used to restore eligible primary maxillary anterior teeth.
Tooth preparation, crown selection, cementation with Fuji IX Extra glass ionomer cement, removal of excess cement, and post-treatment instructions will follow a standardized protocol.
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Experimentell: Bioflx
Participants receive prefabricated Bioflx crowns for restoration of indicated primary maxillary anterior teeth.
Teeth are prepared using a standardized clinical protocol, and crowns are cemented with Fuji IX Extra glass ionomer cement.
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Prefabricated Bioflx crowns manufactured by Kids-e-Dental, India, will be used to restore eligible primary maxillary anterior teeth.
Tooth preparation, crown selection, cementation with Fuji IX Extra glass ionomer cement, removal of excess cement, and post-treatment instructions will follow a standardized protocol.
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Vad mäter studien?
Primära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
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Gingival index
Tidsram: 3, 6, and 12 months after crown placement
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Gingival status adjacent to crowned primary maxillary anterior teeth, assessed using the Löe and Silness Gingival Index.
Lower scores indicate better gingival health.
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3, 6, and 12 months after crown placement
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Fluorescent Plaque Index
Tidsram: 3, 6, and 12 months after crown placement
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Plaque accumulation on crowned primary maxillary anterior teeth, assessed using QrayScan Plus according to the Fluorescent Plaque Index (FPI; 0-5).
Higher scores indicate greater plaque accumulation.
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3, 6, and 12 months after crown placement
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Opposing Tooth Wear
Tidsram: 3, 6, and 12 months after crown placement
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Wear of the tooth opposing the crowned primary maxillary anterior tooth, assessed clinically on a 0-4 ordinal scale.
Higher scores indicate greater enamel and dentin loss.
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3, 6, and 12 months after crown placement
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Crown Retention
Tidsram: 3, 6, and 12 months after crown placement
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Retention status of the prefabricated crown, categorized as retained or loose/lost.
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3, 6, and 12 months after crown placement
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Clinical Status of Crowned Teeth
Tidsram: 3, 6, and 12 months after crown placement
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Clinical status of teeth restored with prefabricated crowns, categorized as asymptomatic, sensitive, mobile, painful, or swollen.
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3, 6, and 12 months after crown placement
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Sekundära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
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Parental Satisfaction
Tidsram: 6 and 12 months after crown placement
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Parental satisfaction with the esthetic outcome of crown restoration, assessed using a 4-point Likert scale for crown shape, color, alignment, interdental spacing, perceived crowding, and other esthetic abnormalities.
Lower scores indicate greater satisfaction.
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6 and 12 months after crown placement
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Samarbetspartners och utredare
Publikationer och användbara länkar
Studieavstämningsdatum
Studera stora datum
Studiestart (Faktisk)
Primärt slutförande (Beräknad)
Avslutad studie (Beräknad)
Studieregistreringsdatum
Först inskickad
Först inskickad som uppfyllde QC-kriterierna
Första postat (Faktisk)
Uppdateringar av studier
Senaste uppdatering publicerad (Faktisk)
Senaste inskickade uppdateringen som uppfyllde QC-kriterierna
Senast verifierad
Mer information
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Ytterligare relevanta MeSH-villkor
Andra studie-ID-nummer
- H2025/387
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