Clinical Trials Logo
  1. Home
  2. Non-carious Cervical Lesions
  3. NCT05945173

Evaluation of the Solvent Evaporation Time of Universal Adhesives in the Quality of Cervical Lesions Restorations

Non-carious Cervical Lesions Clinical Trial

Official title:
Clinical Evaluation of the Effect of the Prolonged Evaporation Time of the Solvent of Two Universal Adhesives in Restorations of Non-carious Cervical Lesions: Double-blind Randomized Clinical Trial

Clinical Trial Summary

The aim of this study will be to evaluate the effect of prolonging solvent evaporation time on the 6- and 12-months clinical performance of two universal adhesive systems used as selective enamel etch (SEE). Methods: 140 restorations will be randomly placed in 35 subjects according to the following groups: SUP5 (Scotchbond Universal Plus evaporated for 5 s); SUP25 (Scotchbond Universal Plus evaporated for 25 s); GBU5 (Gluma Bond Universal evaporated for 5 s); GBU25 (Gluma Bond Universal evaporated for 25 s). Resin composite will be placed incrementally and light-cured. The restorations will be evaluated at baseline, after a week, 6 and 12 months using the FDI and USPHS criteria. Statistical analyses will be performed using appropriate tests (α = 0.05).

Clinical Trial Description

This is a four-arm, double-blind, randomized controlled clinical trial. Experimental group 1: 35 non-carious cervical lesions (NCCL) will receive composite resin restorations using an alcohol- and water-based solvent universal adhesive (Scotchbond Universal Plus; 3M) in the selective enamel etching strategy with evaporation of solvent for 25 seconds. Experimental group 2: 35 non-carious cervical lesions (NCCL) will receive composite resin restorations using an acetone-based universal solvent adhesive (Gluma Universal Bond; Kulzer) in the selective enamel etching strategy with solvent evaporation for 25 seconds. Control group 1: 35 non-carious cervical lesions (NCCL) will receive composite resin restorations, using an alcohol- and water-based universal solvent adhesive (Scotchbond Universal Plus; 3M), in the selective enamel etching strategy, with evaporation of solvent for 5 seconds. Control group 2: 35 non-carious cervical lesions (NCCL) will receive composite resin restorations, using an acetone-based universal solvent adhesive (Gluma Universal Bond; Kulzer), in the strategy of selective enamel etching, with solvent evaporation for 5 seconds. LCNCs will be randomized to universal adhesive usage and flash-off time. All groups will be light-cured with a light-curing device (SmartLite Focus, Dentsply) with a light intensity of 855 mW/cm² for 20 seconds. Operators will restore the cervical area by applying three increments of resin (Opallis, FGM Prod. Odont.Ltda, Joinville, SC, Brazil). Each increment will light cure for 10 s at 1200 mW/cm2 (Radii Cal, SDI, Victoria, Australia). Restorations will be finished immediately with fine diamond burs (#3195F and #3195FF, KG Sorensen, Barueri, SP, Brazil) and polished with discs and polishing gums (Soflex, 3 M ESPE, St. Paul, MN, EE. UU.). ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05945173
Study type Interventional
Source Universidad de los Andes, Chile
Contact
Status Completed
Phase N/A
Start date March 30, 2023
Completion date June 23, 2023
View Details
See also
  Status Clinical Trial Phase
Not yet recruiting NCT06359093 - Prevalence Of Non-Carious Cervical Lesions, Associated Risk Indicators and Salivary Assessment Among Middle Adulthood Patients.
Completed NCT03932929 - 36-Month Clinical Evaluation of a Universal Adhesive N/A
Active, not recruiting NCT04707898 - Clinical Evaluation of Different Universal Adhesive Systems in Non-carious Cervical Lesions. N/A
Active, not recruiting NCT05029479 - the Clinical Performance of a Moisture Resistant, M-TEG-P Phosphate Monomer Based Universal Adhesive (YAMAKIN TMR-Aquabond0) Compared to the Conventional Universal Adhesive (3m ESPE Single Bond Universal Adhesive) N/A
Completed NCT01947192 - Chlorhexidine as Coadjuvant in Dentin Adhesion of Noncarious Cervical Lesions N/A
Completed NCT03637946 - Release of Organic Components of a GIOMER in Non-carious Cervical Lesion Restorations N/A
Active, not recruiting NCT04565938 - Clinical Performance of a One-step Self-etch Adhesive in Non-carious Cervical Lesions at 2 Years Phase 2
Active, not recruiting NCT03086720 - Deproteinization as a Coadjuvant in Dentin Adhesion of Noncarious Cervical Lesions N/A
Completed NCT01506830 - Cervical Restorations Placed Under Two Isolation Methods Phase 2/Phase 3
Recruiting NCT06238999 - Split-mouth Study of a New Flowable Composite in Non-carious Cervical Lesions N/A
Completed NCT03153969 - Clinical Evaluation of a New Giomer Restorative System in Class V Restorations N/A
Not yet recruiting NCT06364020 - Assessment of Risk Factors in Patients With Non-carious Cervical Lesions