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Zirconia Crowns Versus Extraction of Primary Anterior Teeth

Patient-centred, Developmental and Quality-of-life Outcomes Following Zirconia Crown Restoration Versus Extraction of Severely Mutilated Primary Anterior Teeth: a Pragmatic Comparative Clinical Study

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07719478
Enrollment
60
Registered
2026-07-22
Start date
2026-07-18
Completion date
2026-08-01
Last updated
2026-07-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Early Childhood Caries (ECC)

Brief summary

Severely mutilated anterior primary teeth in preschool children are frequently managed by extraction. However, premature loss of anterior primary teeth has been associated with adverse functional, developmental and psychosocial outcomes, including impaired oral health-related quality of life (OHRQoL), speech concerns and negative self-image. Prefabricated zirconia crowns offer an aesthetic and durable restorative alternative for compromised anterior primary teeth. Despite increasing clinical use, comparative evidence evaluating zirconia crown restoration versus extraction under equivalent conditions using validated patient-centred, developmental and economic outcomes remains limited. This pragmatic, prospective, non-randomised controlled clinical study aims to compare zirconia crown restoration and extraction of severely mutilated anterior primary teeth performed under GA in preschool children. Outcomes include OHRQoL, parental satisfaction, child self-image, and speech development.

Detailed description

Early childhood caries (ECC) remains one of the most prevalent chronic conditions in preschool children. Management of decayed anterior primary teeth is particularly challenging due to young age, limited cooperation and extensive tooth destruction. As a result, extraction is often selected as a definitive treatment. However, systematic and rapid reviews have demonstrated associations between premature loss of primary anterior teeth and adverse outcomes, including reduced OHRQoL, speech distortion, altered oral habits and psychosocial impacts. These reviews have consistently highlighted the need for prospective, patient-centred studies employing validated outcome measures and addressing methodological limitations of earlier research. Prefabricated zirconia crowns have emerged as an aesthetic and durable restorative option for anterior primary teeth. While clinical success and parental acceptance have been reported, direct comparisons with extraction that incorporate patient-centred outcomes and economic evaluation are scarce. This study addresses these gaps by prospectively comparing zirconia crown restoration and extraction of decayed anterior primary teeth, using validated OHRQoL, parental satisfaction, child self-image and speech development. Study Design * Allocation: Non-randomised (controlled clinical study) * Blinding: Outcome assessors and data analysts/statisticians will be blinded * Primary Purpose: Treatment * Design Framework: Pragmatic clinical study reflecting routine practice Enrollment 60 participants Arms and Interventions Arm 1: Zirconia Crown Group Intervention: Restoration of decayed anterior primary teeth using prefabricated zirconia crowns. Arm 2: Extraction Group Intervention: Extraction of decayed anterior primary teeth, without anterior prosthetic replacement. Allocation Method: Allocation will be performed based on predefined clinical restorability criteria and shared decision-making with parents or legal guardians. Randomisation will not feasible due to ethical and clinical considerations. Outcome Measures Primary Outcome Measure Change in Oral Health-Related Quality of Life (OHRQoL) * Measurement Tool: Early Childhood Oral Health Impact Scale (ECOHIS), parent-reported * Time Frame: Baseline (pre-treatment), 1 month post-treatment, 3 months post-treatment (primary endpoint) * Units: Total score (0-52) and domain scores * Description: Higher scores indicate poorer OHRQoL Secondary Outcome Measures 1. Parental Satisfaction * Measure: Structured questionnaire * Scale: 5-point Likert scale * Time Frame: 1 month and 3 months 2. Child Self-Image * Measure: Parent-reported pictorial self-image scale * Units: Composite score * Time Frame: 1 month and 3 months 3. Speech Development * Measure: Clinical articulation assessment by a calibrated examiner * Units: Presence or absence of articulation concerns * Time Frame: Baseline and 3 months Eligibility Criteria Inclusion Criteria * Children aged 3-5 years * Presence of one or more decayed primary anterior teeth * Written informed consent from parent or legal guardian Exclusion Criteria * Craniofacial anomalies or genetic syndromes * Diagnosed developmental delay or speech disorders * Previous speech therapy * Systemic disease contraindicating general anaesthesia Study Population Preschool children having decayed anterior primary teeth. Sample Size A total of 60 children (30 per group). Sample size was calculated to detect a clinically meaningful difference in ECOHIS scores with 80% power and a 5% significance level, allowing for attrition. Statistical Analysis Plan * Baseline characteristics described using descriptive statistics * Between-group comparisons using parametric or non-parametric tests as appropriate * Longitudinal OHRQoL changes analysed using repeated-measures models * Statistical significance set at p \< 0.05 Ethics and Safety Ethics Approval The study will be submitted to received approval from Ciro University ethics committee. Informed Consent Written informed consent will be obtained from parents or legal guardians prior to participation. Safety Considerations All procedures represent standard dental care. No additional risk beyond routine clinical practice will be introduced. Risk of Bias Management * Multi-operator pragmatic delivery by non-author clinicians * Automated, anonymised online collection of subjective outcomes * Pre-specified primary endpoint at 3 months * Blinded outcome assessment and statistical analysis

Interventions

Restoration of severely mutilated anterior primary teeth using prefabricated zirconia crowns performed.

PROCEDUREExtraction

Extraction of severely mutilated anterior primary teeth, without anterior prosthetic replacement.

Sponsors

Passant Nagy
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
3 Years to 5 Years
Healthy volunteers
Yes

Inclusion criteria

* Children aged 3-5 years * Presence of one or more decayed primary anterior teeth * Written informed consent from parent or legal guardian

Exclusion criteria

* Craniofacial anomalies or genetic syndromes * Diagnosed developmental delay or speech disorders * Previous speech therapy * Systemic disease contraindicating general anaesthesia

Design outcomes

Primary

MeasureTime frameDescription
Change in Oral Health-Related Quality of Life (OHRQoL)1 month and 3 months* Measurement Tool: Early Childhood Oral Health Impact Scale (ECOHIS), parent-reported * Time Frame: Baseline (pre-treatment), 1 month post-treatment, 3 months post-treatment (primary endpoint) * Units: Total score (0-52) and domain scores * Description: Higher scores indicate poorer OHRQoL

Secondary

MeasureTime frameDescription
1. Parental Satisfaction1 month and 3 months* Measure: Structured questionnaire * Scale: 5-point Likert scale * Time Frame: 1 month and 3 months
2. Child Self-Image1 month and 3 months* Measure: Parent-reported pictorial self-image scale * Units: Composite score * Time Frame: 1 month and 3 months
3. Speech Development1 month and 3 months* Measure: Clinical articulation assessment by a calibrated examiner * Units: Presence or absence of articulation concerns * Time Frame: Baseline and 3 months

Contacts

CONTACTPassant Nagi, A. professor
passant.nagi@dentistry.cu.edu.eg+201120655633
CONTACTAhmed Elkhadem, Professor
Ahmed.elkhadem@dentistry.cu.edu.eg+01064440888
STUDY_CHAIRCairo University Cairo University

Cairo University

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 23, 2026