Skip to content

Resin Polymer (NuSmile BioFlx) Compared to Stainless Steel Crowns (3M ESPE) for Restoration of Primary Molar Teeth

Clinical and Radiographic Success of Resin Polymer (NuSmile BioFlx) Compared to Stainless Steel (3M ESPE) Crowns for Restoration of Primary Molar Teeth: a Split Mouth Randomized Controlled Trial.

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06354634
Enrollment
28
Registered
2024-04-09
Start date
2024-06-07
Completion date
2025-02-01
Last updated
2025-02-26

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

Conditions

Dental Caries, Tooth Decay

Brief summary

The purpose of this research study is to test the effectiveness of two different crowns/caps on teeth for restoration of primary molar teeth. The two different materials of crowns are resin polymer and stainless steel crowns. These crowns are placed on the teeth to restore function and prevent further caries and infection.

Detailed description

There is a lack of literary evidence for assessment of the properties of Bioflx crowns and their effect on clinical outcomes and parental satisfaction compared to traditionally available options including stainless steel crowns and zirconia crowns. Hence, this study plans to assess the clinical performance and child and parental satisfaction of Bioflx compared to the gold standard stainless steel crowns in pediatric patients.

Interventions

OTHERResin polymer (NuSmile Bioflx) crown

Resin polymer (NuSmile Bioflx)crown

Stainless steel crown

Sponsors

Virginia Commonwealth University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

Each participant will receive both interventions.

Eligibility

Sex/Gender
ALL
Age
3 Years to 7 Years
Healthy volunteers
No

Inclusion criteria

* Age: Children age group 3-7 yrs old * Primary molars affected with caries or hypoplastic defect. * Occlusion: Primary molar must have antagonist tooth. * Consent of parent (legal guardians) and child assent for 7 years. * Multi-surface dental caries observed in more than one tooth, in either side of the same arch (maxilla or mandible) or opposite arch (maxilla or mandible) * Status: Asymptomatic or symptomatic teeth with signs of reversible pulpitis

Exclusion criteria

* Teeth with advanced stages of resorption (more than 2/3rd) * Teeth exhibiting irreversible pulpitis. * Teeth for which pulpotomy is done. * Molar in infraocclusion * Medically compromised children (ASA 3 or 4) * History of grinding or pathological attrition * Adverse gingival or periodontal conditions

Design outcomes

Primary

MeasureTime frameDescription
The success of Bioflx crown in primary molars in comparisons with stainless steel molars through clinical assessments3, 6, 12, 18, 24 and 36 monthsThe clinical outcomes will be measured and reported in the data table based on the number of participants scored on 3-point Likert scale (Ideal, Acceptable, or Not Acceptable) for the following parameters separately: Contour of crown, gingival health, staining of crown, surface roughness of crown, opposing tooth, color match of crown, marginal fit, marginal discoloration, recurrent caries.
The success of Bioflx crown in primary molars in comparisons with stainless steel molars through radiographic assessments3, 6, 12, 18, 24 and 36 monthsThe radiographic outcomes will be measured and reported in the data table based on the number of participants scored on either presence or absence (yes / no) of the findings for the following parameter separately: Widening of periodontal ligament space, furcation radiolucency, periapical pathology, alveolar crestal bone loss, internal root resorption and external root resorption.

Secondary

MeasureTime frameDescription
Parental satisfaction3, 12, 24 and 36 monthsThe questionnaire is a Likert scale of 1-5. 1 equals very dissatisfied. 5 equals very satisfied. The higher the score, the better.
Child satisfaction3, 12, 24 and 36 monthsThe questionnaire is a Likert scale of 1-5. 1 equals very dissatisfied. 5 equals very satisfied. The higher the score, the better.
ECOHIS (Early Childhood Oral Health Impact Scale) surveyPre-operative, 6, 12, 24 and 36 monthsThe questionnaire is a Likert scale of 1-5. 1 equals never. 5 equals very often. The lower the score, the better.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026