Preparation Time Of Bioflx Crowns Compared To Zirconia Crowns On Primary Molars
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: bioflx crown, zirconia crown.
- Who it may be relevant to
- Registry conditions: Carious Primary Molars. Basic parameters: 4 years — 8 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Egypt
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Official title
Evaluation Of Preparation Time Of Bioflx Crowns Compared To Zirconia Crowns On Primary Molars
Overview
This study aims to evaluate and compare the preparation time required for Bioflx crowns versus zirconia crowns on primary molars through a randomized clinical trial. • Primary Objective: To compare the preparation time required for Bioflex crowns and zirconia crowns on primary molars in pediatric patients. • Secondary Objectives: To evaluate the clinical performance of Bioflex crowns compared to zirconia crowns, including: Retention, Patient Satisfaction, Parental Satisfaction, Occlusal Wear and Gingival Health. the main question it aim to answer: Is there a significant difference in the preparation time required for Bioflx crowns compared to zirconia crowns in the primary molars of pediatric patients?
Detailed description
In pediatric dentistry, achieving efficient and aesthetic restoration of primary molars remains a significant challenge, particularly when treating young or anxious patients who may struggle with long or complex procedures. Zirconia crowns are widely used due to their durability, excellent biocompatibility, and natural tooth-like appearance, making them the gold standard for full-coverage aesthetic restorations in children. However, their placement involves extensive tooth preparation, which results in longer chair time and an increased risk of pulp exposure. These factors can negatively impact both treatment outcomes and patient behavior management.
Bioflex crowns have emerged as a potential alternative, offering a more flexible and user-friendly design that simplifies placement and reduces the amount of tooth preparation required. This may result in shorter procedure times and improved patient comfort. Despite these potential benefits, there is currently limited clinical evidence comparing the preparation time and efficiency of Bioflex crowns versus zirconia crowns for restoring primary molars.
This gap in knowledge makes it difficult for clinicians to make fully informed decisions about which crown system offers the best balance of procedural efficiency, aesthetics, and patient cooperation. By directly comparing Bioflex and zirconia crowns in terms of tooth preparation time and overall clinical practicality, the proposed study aims to determine whether Bioflex crowns provide a significant advantage in pediatric settings. The results could help identify the most time-efficient and effective restorative option for primary molars, ultimately improving care outcomes for pediatric patients.
Interventions
- Other bioflx crown
(Group A: Preformed Biofix Crown - Assigned Intervention) Crown Selection \& Tooth Preparation: Measure the mesiodistal width using calipers to select an appropriately sized crown. If a mesial or distal wall is missing, use the contralateral tooth for size selection. Choose the crown that closely matches the measured mesiodistal width. Select the smallest crown that preserves proximal contacts using a trial-and-error approach. If crimping is necessary, use Howe's pliers. Perform 1-1.5 mm occl - Other zirconia crown
Group B: Preformed Zirconia Crown - Assigned Intervention) Crown Selection: Measure the mesiodistal width using calipers to select the appropriate crown. If a mesial or distal wall is missing, use the contralateral tooth for size selection. Choose the one that closely matches the mesiodistal width. Select the smallest crown that preserves proximal contacts. Tooth Preparation: Reduce the occlusal surface by 1.5-2 mm using a tapered diamond bur. Reduce interproximal areas by 1-1.5 mm, ensurin
Primary outcome measures
- prepration time [Time frame: time frame: T0: 0 basline, follow up 12 month]
Secondary outcome measures (4)
- Occlusal wear of crown [Time frame: T (Time): 12 months Intervals: T0: 0, T1: 3 months, T2: 6 months, T3: 12 months]
- retention [Time frame: Follow-up: 12 months Intervals: T0: 0, T1: 3 months, T2: 6 months, T3: 12 months]
- Gingival Health [Time frame: 12 months Intervals: T0: 0, T1: 3 months, T2: 6 months, T3: 12 months]
- Child and parental satisfaction [Time frame: T (Time): 12 months Intervals: T0: 0, T1: 3 months, T2: 6 months, T3: 12 months]
Eligibility criteria
Inclusion criteria
- Children aged between 4 and 8 years with a primary molar that needs to be covered by a crown.
Medically healthy children (ASA I or II according to the American Society of Anesthesiologists classification).
Children whose parent or guardian is willing to sign an informed consent.
Children whose parent or guardian are willing to comply with follow-up visits.
Frankl's positive and definitely positive patient.
Exclusion criteria
- Molars with severe structural loss that may compromise crown retention.
Children with poor oral hygiene that may contribute to higher plaque levels and affect the clinical outcomes of the crown restorations.
Children with a history of allergies; known allergies to dental local anesthesia or to the materials used in Biofix crowns.
Children with any systemic conditions or disabilities that may affect their ability to participate in the study.
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: Yes
Study design
- Allocation
- Randomized
- Model
- Parallel assignment
- Masking
- Single blind
- Primary purpose
- Treatment
Study locations
Egypt · 1 center
- Faculty of Dentistry Cairo University — Cairo
Identifiers
NCT: NCT06968767 · PT-BFC VS ZRC