Skip to content

Clinical performance of flowable resin composites with bioactive technology and resin-modified glass ionomer cement in noncarious cervical lesions of abfraction: a randomized control clinical trial

Clinical performance of flowable resin composites with Giomer technology and resin-modified glass ionomer cement in abfraction lesions: a randomized control clinical trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-8yqbfr
Enrollment
Unknown
Registered
2020-08-31
Start date
2020-10-10
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

Tooth Wear

Interventions

Sponsors

Faculdade de Odontologia de Bauru, Universidade de São Paulo
Lead Sponsor
Faculdade de Odontologia de Bauru, Universidade de São Paulo
Collaborator

Eligibility

Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Participants must be between 18 and 65 years of age; have good oral hygiene; absence of periodontal disease; have at least 20 teeth in occlusion and of these three or more teeth must present noncarious cervical lesions (NCL) of the abfraction type; the lesions should be approximately 2 mm deep.

Exclusion criteria

Exclusion criteria: Participants with caries activity; unsatisfactory oral hygiene conditions; severe bruxism or other parafunctional habits; periodontal disease and systemic complications; participants who have undergone orthodontic or hypersensitivity treatments in the past six months will be excluded; in addition to pregnant and lactating women; teeth with abfraction lesions that have an implant or total prosthesis as an antagonist will also not be included in the research.

Design outcomes

Primary

MeasureTime frame
Evaluate the retention of restorations using the modified USPHS and FDI methods. The restorations will be evaluated by two blind examiners and calibrated in the baseline periods (7 days), 6 months, 1, 3 and 5 years.

Secondary

MeasureTime frame
Assess color, marginal pigmentation, caries, wear, marginal adaptation of restorations using the modified USPHS and FDI methods. The restorations will be evaluated by two blind examiners and calibrated in the baseline periods (7 days), 6 months, 1, 3 and 5 years.;Assess the level of postoperative sensitivity using the visual analogic scale (VAS). The postoperative sensivity will be evaluated by two blind examiners and calibrated in the baseline periods (7 days), 6 months, 1, 3 and 5 years.

Countries

Brazil

Contacts

Public ContactLinda Wang

Faculdade de Odontologia de Bauru, Universidade de São Paulo

wang.linda@usp.br+55(14)32358480

Outcome results

None listed

Source: REBEC (via WHO ICTRP)