MedPath

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
Completed
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
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod

MedPath

Empowering clinical research with data-driven insights and AI-powered tools.

© 2025 MedPath, Inc. All rights reserved.