Clinical evaluation of a universal adhesive in total-etch and selective-etch modes in the restoration of non-carious cervical lesions in Nigerian adults

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Interventional

Source

PACTR

Registry ID

PACTR202308672010618

Enrollment

Registered

2023-08-28

Start date

2020-09-13

Completion date

Unknown

Last updated

2026-09-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Non-carious cervical lesions of the teeth

Interventions

Total etch mode

Selective etch mode

Eligibility

Sex/Gender

All

Inclusion criteria

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

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.

Design outcomes

Primary

Measure	Time frame
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

Measure	Time frame
The use of universal adhesives for composite restoration performed excellently in both modes of placement in this study.	—

Countries

Nigeria

Contacts

Public ContactAdenike Awotile

Consultant

nikawo2008@yahoo.com+2348033256281

Outcome results

None listed

Source: PACTR (via WHO ICTRP) · Data processed: Sep 19, 2026