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Impact of different Materials on the gum of teeth with Lesions near the gums that are not caused by Caries

Impact of different Composite Resins on the Periodontal response of teeth with Non-Carious Cervical Lesions: randomized controlled clinical trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-5spkfw2
Enrollment
Unknown
Registered
2025-10-03
Start date
2025-09-01
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 Abrasion

Interventions

This is a randomized controlled clinical trial, using a split-mouth design, with equal allocation between groups and a double-blind approach, aimed at evaluating the characteristics of restorative mat

Sponsors

Faculdade de Odontologia da Universidade Federal de Uberlândia
Lead Sponsor
Faculdade de Odontologia da Universidade Federal de Uberlândia
Collaborator

Eligibility

Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Participant must be at least 18 years old; both sexes; must have a clinical diagnosis of non-carious cervical lesion with a cavity depth between 1.0 mm and 2.0 mm, located on the buccal surface of at least three premolar teeth; teeth must be non-mobile; participants must be in good general health (ASA I: a normal healthy patient; and ASA II: a patient with mild systemic disease without significant functional limitations); must maintain acceptable oral hygiene according to the Simplified Oral Hygiene Index (OHI-S); must have at least 20 teeth in occlusion; the cavosurface margin must involve more than 50% enamel

Exclusion criteria

Exclusion criteria: Participants with a history of allergy to any material used in the study; smoking participants; participants requiring gingival grafting in the region of the teeth to be treated; use of orthodontic appliances; severe or chronic periodontitis (evidenced by pocket depth greater than 4 mm with bleeding on probing and clinical attachment loss greater than 3 mm in more than 4 teeth); teeth with Miller Class III or IV gingival recession; severe bruxism (characterized by significant masticatory muscle pain, temporomandibular joint pain, or extreme tooth wear); pregnant or breastfeeding women

Design outcomes

Primary

MeasureTime frame
To evaluate whether composite resins will have different impacts on gingival inflammation, using the gingival inflammation index as a parameter, based on the observation of a 10% variation in the degree of inflammation between the resins

Secondary

MeasureTime frame
To evaluate whether composite resins will exhibit distinct behaviors regarding functional, biological, and esthetic properties, as assessed by the World Dental Federation (FDI) criteria, in the event of changes of approximately 10% between the composite resins

Countries

Brazil

Contacts

Public ContactMurilo de Sousa Menezes

Faculdade de Odontologia da Universidade Federal de Uberlândia

murilomenezes@ufu.br+55 34 3225-8106 R:8106

Outcome results

None listed

Source: REBEC (via WHO ICTRP)