Status:
UNKNOWN
Evaluation of Organically Modified Ceramic Resin Composite Versus Bulkfill Resin in Proximal Posterior Cavities
Lead Sponsor:
Cairo University
Conditions:
Proximal Caries
Eligibility:
All Genders
18-60 years
Phase:
NA
Brief Summary
In patients with compound posterior proximal cavities, will the use of organically modified ceramic resin composite restorative material have similar clinical performance to conventional bulk fill res...
Detailed Description
The study will be conducted in the clinic of Conservative Dentistry Department, Faculty of Dentistry, Cairo University; the operator in charge Safinaz Hussien ,The subjects fulfilling the eligibility ...
Eligibility Criteria
Inclusion
- Patients aging ≥18 years.
- Patients with a high level of oral hygiene.
- Patients having at least 1or 2 posterior teeth in occlusion.
- Patients with good likelihood of recall availability.
- Tooth inclusion:
- Permanent premolars or molars.
- Moderate to deep compound class II cavities.
- Primary carious lesions.
- Vital with positive reaction to cold thermal stimulus.
- Well-formed and fully-erupted in normal functional occlusion with natural antagonist and adjacent teeth.
Exclusion
- Participants with general/systemic illness.
- Pregnant or lactating females.
- Concomitant participation in another research study.
- Inability to comply with study procedures.
- Heavy bruxism habits.
- Last experience with allergic reactions against any components of the used materials.
- Patients receiving orthodontic treatment.
- Tooth exclusion:
- Teeth with clinical symptoms of pulpitis such as spontaneous pain or sensitivity to pressure.
- Non-vital teeth.
- Secondary carious lesions.
Key Trial Info
Start Date :
January 1 2021
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
February 1 2022
Estimated Enrollment :
22 Patients enrolled
Trial Details
Trial ID
NCT04677023
Start Date
January 1 2021
End Date
February 1 2022
Last Update
December 23 2020
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