Occlusal Wear Of Bioflx Crowns Compared To Zirconia Crowns On Primary Molars
ConditionCarious Primary Molars
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age4-8
SponsorCairo University
About this trial
The goal of this clinical trial is to evaluate the occlusal wear of Bioflx crowns compared to zirconia crowns in the restoration of primary molars.
The main question\[s\] it aims to answer : " Is there a difference in the occlusal wear of BioFlx crowns compared to zirconia crowns in the restoration of primary molars?" The study will also assess the clinical performance of both types of crowns in terms of retention,gingival health, preparation time, as well as child and parental satisfaction.
Eligibility criteria
Qualifiers
Children aged between 4 and 8 years with primary molar that needs to be covered by crown.
Medically healthy children (ASA I or II according to the American Society of Anesthesiologists classification).
Children whose parent or guardian are willing to sign an informed consent.
Children whose parent or guardian are willing to comply with follow-up visits. -
Disqualifiers
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 history of allergies; Known allergies to dental local anesthesia or to the materials used in Bioflx crowns.
Children with any systemic conditions or disabilities that may affect their ability to participate in the study.
Trial design
Treatments tested in this trial
- (Group A: Preformed Bioflx Crown)
- (Group B: Preformed Zirconia crown)
Treatment groups
50 Participants
are divided into 2 treatment groupsLocations
1Map coordinates are unavailable for these locations. Locations are shown below instead.
Faculty of dentistry cairo university Status unavailable 12613, Cairo ,Giza, Egypt
Egypt
EgyptSponsors and collaborators
Source ClinicalTrials.gov