Clinical evaluation of a universal adhesive in total-etch and selective-etch modes in the restoration of non-carious cervical lesions in Nigerian adults
Phase 1
- Conditions
- Non-carious cervical lesions of the teeth
- Registration Number
- PACTR202308672010618
- Lead Sponsor
- Dr. Temitope Omosebi
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 30
Inclusion Criteria
Subjects aged 18 years and above
Subjects who were available for follow-up visits
Subjects with two non-carious cervical lesions of between 1mm and 3mm depth
Lesions beyond the enamel extending to dentin.
Exclusion Criteria
Subjects with rampant uncontrolled caries.
Subjects with advanced untreated periodontal diseases.
Tooth with periapical pathology.
Non-vital tooth or previous root canal therapy.
Evidence of severe bruxism, clenching and temporomandibular disorder.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The total-etch and selective-etch groups of universal adhesive showed acceptable clinical performance in aesthetic properties, functional properties, and biological effects in the restoration of non-carious cervical lesions throughout the evaluation period.
- Secondary Outcome Measures
Name Time Method The use of universal adhesives for composite restoration performed excellently in both modes of placement in this study.