Status:
UNKNOWN
Evaluation of Ion Releasing Hybrid Restorative Material
Lead Sponsor:
Cairo University
Conditions:
Dental Caries
Eligibility:
All Genders
25-40 years
Phase:
NA
Brief Summary
Esthetic and mechanical evaluation of calcium and phosphate releasing hybrid restorative material and fluoride releasing hybrid restorative material versus the conventional nanofilled resin composite ...
Detailed Description
3 groups of 45 patients will receive class II restorations by using calcium and phosphate releasing hybrid restorative material (Activa Presto), fluoride releasing hybrid restorative material (Giomer)...
Eligibility Criteria
Inclusion
- Patient-related criteria:
- Patients consulting in one of the outpatient clinics listed above.
- Patients can tolerate necessary restorative procedures.
- Provide informed consent.
- Patients accept the one year follow-up period.
- Patients are within middle age group (25-40years).
- Cooperative patients.
- Patients don't have any medically compromised conditions.
- Tooth related criteria:
- Teeth with primary proximal carious lesions in posterior teeth with no pulpal involvement.
- Teeth should have contact with the adjacent teeth.
- Teeth are vital according to pulp-sensitivity tests.
- No active gingival or periodontal conditions.
Exclusion
- • Medically compromised patients, as they will not be able to attend multiple appointments or may require special management.
- Pregnant women; as radiographs are prohibited.
- Allergic Patients to any of the restorative materials, including anesthetics.
- Uncooperative patients will not follow the instructions or attend the appointments.
- Tooth related criteria:
- Retained deciduous teeth; as the research 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) indicating irreversible pulpitis.
- Negative sensitivity tests, periapical radiolucencies, and sensitivity to axial or lateral percussion indicating 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 :
October 10 2021
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
October 30 2022
Estimated Enrollment :
45 Patients enrolled
Trial Details
Trial ID
NCT04854655
Start Date
October 10 2021
End Date
October 30 2022
Last Update
September 9 2021
Active Locations (0)
Enter a location and click search to find clinical trials sorted by distance.
No Results Found
We couldn’t find results for the location/zipcode entered or within the selected range. Please check your input or adjust your search.