Status:
NOT_YET_RECRUITING
Clinical Performance of ARS Containing Universal Adhesives in Carious Cervical Lesions
Lead Sponsor:
Cairo University
Conditions:
Carious Lesion
Cervical Caries
Eligibility:
All Genders
21-67 years
Phase:
NA
Brief Summary
Evaluation of composite restorations done in carious cervical lesions restored by a conventional universal adhesive in comparison to a universal adhesive that contains and resistant silane coupling ag...
Detailed Description
The presence of acidic monomers in the bottle during storage can lead to the hydrolysis of silane contained in universal adhesives, potentially reducing its effectiveness and causing instability,The a...
Eligibility Criteria
Inclusion
- Participants Inclusion:
- • Adults aging from 21-67 years old who were in need of restoration of at least one notch-shaped cervical lesion
- Teeth Inclusion:
- Vital teeth with carious cervical lesions in incisors , canines ,premolars\& molars
Exclusion
- Participants Exclusion:
- Patients with fewer than 20 teeth
- Poor oral hygiene
- Uncontrolled periodontal disease
- Xerostomia
- Known allergy to resin-based materials
- Medically compromised, pregnant, or breast-feeding
- Teeth Exclusion:
- Non vital teeth
- Teeth that are out of occlusion
- Previously restored teeth
Key Trial Info
Start Date :
September 1 2024
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
April 30 2026
Estimated Enrollment :
80 Patients enrolled
Trial Details
Trial ID
NCT06572124
Start Date
September 1 2024
End Date
April 30 2026
Last Update
September 4 2024
Active Locations (1)
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1
Cairo University
Cairo, Egypt