Overview
Clinical Evaluation of Giomer Based Injectable Resin Composite Versus Resin Modified Glass Ionomer in Class V Carious Cavities Over Two Years.
Status:
Not yet recruiting
Not yet recruiting
Trial end date:
2024-08-01
2024-08-01
Target enrollment:
0
0
Participant gender:
All
All
Summary
Class V carious lesions will be restored using either Resin modified glass ionomer or Giomer based injectable resin composite.The restorations will be evaluated at baseline and regular recalls of 3 months, 6 months, 12 months, 18 months and 24 months, using modified United States Public Health Service criteria.Phase:
Phase 1/Phase 2Accepts Healthy Volunteers?
Accepts Healthy VolunteersDetails
Lead Sponsor:
Cairo University
Criteria
Participant Inclusion Criteria- Age 18-60 years.
- Co-operative patients approving to participate in the study.
- Male or female patients.
- Patients with good general health
- Moderate or high caries risk patient
Teeth Inclusion Criteria
- Cervical Class V carious lesions.
- Pulp asymptomatic vital carious teeth.
Participant Exclusion Criteria
- Systemic disease or severe medical complications.
- Participants with a history of allergy to any component of restorations will be used
in the study.
- Lack of compliance
- Evidence of severe bruxism, clenching, or temporomandibular joint disorders or bizarre
habits
Teeth Exclusion Criteria
- Presence of apical or periapical pathosis.
- tooth mobility
- Non-vital teeth.
- Teeth with advanced periodontal diseases.
- Teeth which need indirect restoration.