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Effect of extracted natural agent of grape seed on the longevity of adhesive restorations: clinical trial

Effect of the proanthocyanidin on the longevity of adhesive restoration: randomized and double-blind clinical trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-366mbj
Enrollment
Unknown
Registered
2016-01-04
Start date
2014-11-01
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 wear,non-carious cervical lesions, Dental Materials, retention

Interventions

Forty- five subjects with at least five non-carious cervical lesions are selected. In each individual, the teeth will be randomly divided into 5 groups and given the following treatments: 1) a conven
2) A 2% proanthocyanidin solution (PA) will be applied to the dentin before to application of adhesive (even in the control group
)3) A 5% PA solution will be applied to the dentin before to application of the adhesive (even in the control group)
4 ) PA is included in the commercial adhesive system at a concentration of 2% and will be applied to the dentin 5) PA is included in the commercial adhesive system at a concentration of 5 % and will
Procedure/surgery

Sponsors

Universidade Federal do Ceará
Lead Sponsor
Universidade Federal do Ceará
Collaborator

Eligibility

Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Patients older than 18 years, with good general health, acceptable oral hygiene, with return periods of availability in the evaluation and who have at least 5 teeth with non carious cervical lesions - NCCLs; The teeth with lesions should have a normal occlusal relationship with the antagonist, not present prior restorative treatment; The wells should not be latched with minimum depth of 0.5 mm and mesiodistal width minimum of 1 mm.

Exclusion criteria

Exclusion criteria: Patients who have dental caries, periodontal problems, dry mouth, bruxism. Pregnant; breastfeeding; patients who are undergoing orthodontic treatment; teeth with sharp occlusal stress.

Design outcomes

Primary

MeasureTime frame
Retention: Evaluation through visual inspection with explorer and mirror in periods of 6, 12, 18, 24 months. Will be classified as: retained ou missing.

Secondary

MeasureTime frame
Marginal adaptation: Evaluation through visual inspection with explorer and mirror, if necessary, in periods of 6, 12, 18, 24 months. Will be classified as: Restoration is continuous with existing anatomic form, detectable V-shaped defect in enamel only (catches explorer going both ways) or detectable V-shaped defect to dentinenamel junction Marginal staining: Evaluation through visual inspection with mirror, in periods of 6, 12, 18, 24 months. Will be classified as: no discoloration along the shore, light and superficial staining (removable and usually located) or deep pigmentation that can not be removed by polishing Secondary caries: Evaluation through visual inspection with mirror and explorer, in periods of 6, 12, 18, 24 months. It will be classified as: No evidence of caries contiguous with the margin or evidence of the presence of caries. Postoperative Sensitivity Evaluation by an air jet directed on the restoration at a distance of 3 cm from the tooth surface for 5 seconds, in periods of 6, 12, 18, 24 months. It will be classified as: without postoperative sensitivity immediately after the restorative process and during the study period and this sensitivity at any time during the study period

Countries

Brazil

Contacts

Public ContactVicente de Paulo Saboia

Universidade Federal do Ceará

vpsaboia@yahoo.com+55 (85) 98807.4623

Outcome results

None listed

Source: REBEC (via WHO ICTRP)