Status:
COMPLETED
Clinical Evaluation of Fiber Reinforced Resin Composite Base Versus Incremental Packing of Nanohybrid Resin Composite
Lead Sponsor:
Cairo University
Conditions:
Caries Class II
Eligibility:
All Genders
18-50 years
Phase:
EARLY_PHASE1
Brief Summary
A clinical trial, comparing two different incrementation techniques in the restoration of proximal caries in permanent posterior teeth . One utilizes a fiber reinforced bulk fill base material, follow...
Detailed Description
The aim of this study is to conduct an RCT to evaluate the clinical performance of the fiber reinforced bulk fill resin composite in comparison to incremental packing of nanohybrid resin composite. E...
Eligibility Criteria
Inclusion
- Patient-related criteria:
- Patients consulting in one of the outpatient clinic listed above.
- Able to tolerate necessary restorative procedures.
- Provide informed consent.
- Accepts the one year follow-up period.
- Tooth related criteria:
- Teeth with primary deep carious lesions involving 2/3 of the entire dentin thickness with no continuity between the carious cavity and the pulp chamber.
- Teeth are vital according to pulp-sensitivity tests.
Exclusion
- Patient-related criteria:
- Medically compromised patients, as they will not be able to attend multiple appointments or may require special management.
- Pregnant women; as radiographs cannot be taken for them.
- Allergy to any of the restorative materials, including anesthetics.
- Uncooperative patients, will not abide by the instructions or attend the appointments.
- Tooth related criteria:
- Deciduous teeth; as the study is targeting only permanent teeth.
- Teeth with previous restorations, which may add another variable to the study (type of old restorative material, extent of recurrent caries).
- Spontaneous pain or prolonged pain after sensitivity tests (cold and electrical tests), which would indicate irreversible pulpal damage.
- Negative sensitivity tests, periapical radiolucencies and sensitivity to axial or lateral percussion, which would indicate pulp necrosis.
- Teeth presenting external or internal resorption, with adverse pulpal reactions which may affect the outcome of the study.
- Teeth with cervical caries; which can't be evaluated on periapical radiographs
Key Trial Info
Start Date :
September 1 2020
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
September 30 2021
Estimated Enrollment :
36 Patients enrolled
Trial Details
Trial ID
NCT04019145
Start Date
September 1 2020
End Date
September 30 2021
Last Update
November 9 2021
Active Locations (1)
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1
Cairo University
Cairo, Egypt