Status:
UNKNOWN
Clinical Evaluation of Self- Adhesive Bulk-fill Resin Composite Versus Conventionally Bonded Bulk-fill Resin Composite in Restoration of Proximal Lesions
Lead Sponsor:
Cairo University
Conditions:
Dental Caries Class II
Eligibility:
All Genders
18-100 years
Phase:
NA
Brief Summary
This study will be conducted to evaluate and compare the clinical performance of Self- Adhesive Bulk fill Resin Composite Versus Conventionally Bonded Bulk fill resin composite in Restoration of Proxi...
Detailed Description
A) Participants, interventions \& outcomes 9. Study setting Study will be conducted in the Conservative Dentistry Department, Faculty of Dentistry - Cairo University. 10\. Eligibility criteria 10.a.1...
Eligibility Criteria
Inclusion
- \-
- Patient-related criteria:
- Patients consulting in one of the outpatient clinics listed above.
- Able to tolerate necessary restorative procedures.
- Provide informed consent.
- Accepts the 18 months follow-up period.
- Tooth related criteria:
- Teeth with primary proximal carious lesions .
- 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 :
June 15 2021
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
May 15 2023
Estimated Enrollment :
40 Patients enrolled
Trial Details
Trial ID
NCT04888676
Start Date
June 15 2021
End Date
May 15 2023
Last Update
October 18 2022
Active Locations (1)
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1
Mohamed Mohamed sabry Mohamed
Cairo, Nasr City, Egypt, 11311