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Clinical performance of composite resin restorations in Non-Carious Cervical Lesions

Clinical performance of restorations of non-carious cervical lesions in posterior teeth with bulk-fill composite resins: Randomized clinical trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-7khws8d
Enrollment
Unknown
Registered
2025-04-17
Start date
2023-11-15
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

Erosion

Interventions

This is a randomized, controlled, double-blind, split-mouth clinical study. Experimental group: 39 volunteers aged 18 years or older will receive three dental restorations with Bulk-Fill resins (Filte
D05.750.716.822.308

Sponsors

Universidade de Pernambuco
Lead Sponsor
Universidade de Pernambuco
Collaborator

Eligibility

Age
18 Years to 64 Years

Inclusion criteria

Inclusion criteria: Presence of 4 vital teeth with non-carious cervical lesions on the vestibular surface of premolars and molars; age range from 18 to 64 years; both sexes; present at least 20 teeth; occlusal contact with healthy or properly restored antagonist tooth

Exclusion criteria

Exclusion criteria: Advanced periodontal disease; teeth with pulp alteration or endodontic treatment; participants undergoing orthodontic treatment; severe bruxomas; smokers; participants who make chronic use of analgesics; teeth with tissue loss in the cervical region due to carious lesions; participants with a thin gingival biotype; medical, psychiatric or pharmacotherapeutic history that may compromise the protocol, including chronic use of anti-inflammatory, analgesic and psychotropic drugs; pregnancy or breastfeeding; allergies and idiosyncratic responses to the composition of the products; abutment teeth of fixed or removable prostheses; teeth or support structures with any painful pathology; poor oral hygiene

Design outcomes

Primary

MeasureTime frame
To analyze the clinical performance of composite resin restorations performed, assessed using the criteria of the United States Public Health Service and the criteria of the International Dental Federation. Data will be collected immediately after the restorative protocol, at 6 months, at 12 months and at 18 months.—

Secondary

MeasureTime frame
To assess the dental sensitivity of restored teeth using a visual analogue scale and a pain assessment scale. Data will be collected before the restorative procedure, immediately after, and at 6 months, 12 months, and 18 months.—

Countries

Brazil

Contacts

Public ContactAna Luisa Bezerra

Universidade de Pernambuco

analuisa.bezerra@upe.br+55 81 99882-9964

Outcome results

None listed

Source: REBEC (via WHO ICTRP)