Clinical Trials Directory

Trials / Unknown

UnknownNCT05861193

Treatment of NCCL Asociated With Gingival Recession With B.O.P.T. Technique

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
25 (estimated)
Sponsor
University of Valencia · Academic / Other
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Accepted

Summary

The purpose of this clinical trial is to evaluate the gingival margin changes resulting from the treatment with biologically oriented preparation technique (B.O.P.T.) of non-carious cervical lesions (NCCL). In particular, the quantification of the cervical margin is carried out by an intraoral scanning device, both in length and width.

Conditions

Interventions

TypeNameDescription
PROCEDURETreatment of the abfraction with BOPT techniqueThe steps to follow for the treatment of abfraction using composite resin and the B.O.P.T. technique will consist of: * Selection of the color of the composite, placement of the retraction cord and chamfering of the coronal margin of the lesion; * Application of 37% phosphoric acid etching and adhesive in 3 steps; placement of the composite by layers, following the conventional obturation technique. * Execution of an overfilling with the composite at the level of the cervical emergence profile of the tooth, with the aim of emphasizing said anatomical particularity. * Removal of the retraction cord. * Diamond milling with red rim flame diamond bur and contra-angle, positioned from the most apical point of the restoration at an angle of 45º without touching the restored dental portion, with the aim of performing a level rotary gingival curettage from the margin of the restoration. * Polishing with a fine-grain flame bur, and polishing discs of decreasing granulometry.

Timeline

Start date
2022-09-20
Primary completion
2023-05-20
Completion
2023-07-01
First posted
2023-05-16
Last updated
2023-05-16

Locations

1 site across 1 country: Spain

Source: ClinicalTrials.gov record NCT05861193. Inclusion in this directory is not an endorsement.