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Clinical evaluation of dental adhesives applied in different techniques in non-carious cervical lesions

Clinical Evaluation of Clearfil S3 Bond Universal Quick applied in different techniques in non-carious cervical lesions

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-69p7mpr
Enrollment
Unknown
Registered
2022-06-09
Start date
2022-04-04
Completion date
Unknown
Last updated
2025-10-27

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

Conditions

Dentin hypersensitivity, root caries

Interventions

no drugs. 150 restorations will be performed in a 150 teeth, using the following adhesive techniques: “No-Waiting Technique" Group (50) – where the Clearfil S3 Bond Universal Quick adhesive (Kuraray N
D017220

Sponsors

Andres Felipe felipe Millan Cardenas
Lead Sponsor
Centro Universitário de Maranhão - UNICEUMA
Collaborator

Eligibility

Age
18 Years to 50 Years

Inclusion criteria

Inclusion criteria: Age between 18-50 years old; Participants must have at least three comparable LCNCs (in size, shape, and dimensions) to be restored; These lesions must be non-retentive, deeper than 1 mm, and involve both enamel and dentin of vital teeth without periodontal disease; Acceptable oral hygiene and have at least 20 teeth under occlusion.

Exclusion criteria

Exclusion criteria: The cavo-superficial margin cannot involve more than 50% of the enamel; Extremely poor oral hygiene or using orthodontic treatment; Severe or chronic periodontitis or heavy bruxism habits; Known allergy to resin-based materials or any other material used in this study; Pregnant or lactating women; Patients with chronic use of anti-inflammatory, analgesic and psychotropic drugs.

Design outcomes

Primary

MeasureTime frame
restoration retention/fracture after clínical evaluation and according to International Federation (FDI) and classical United States Public Health Service (USPHS)

Secondary

MeasureTime frame
The evaluation of spontaneous postoperative sensitivity will be performed one week after the restorative procedure, asking the patient if he/she felt any pain during the period.

Countries

Brazil

Contacts

Public Contactandres millan cardenas

Centro Universitário de Maranhão - UNICEUMA

andresfelipemillancardenas@hotmail.com9898574270

Outcome results

None listed

Source: REBEC (via WHO ICTRP) · Data processed: Feb 9, 2026