Different Application Strategies When Using Futurabond Universal in Class V Cavities
NCT03244124 · Status: ACTIVE_NOT_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 50
Last updated 2026-05-15
Summary
Treatment clinical trial, randomized, controled, parallel, double-blinded, with four groups, that aims to evaluate the best application strategy when using a new Universal Adhesive system, Futurabond Universal (VOCO GmbH, Germany). Volunteers will be selected and recruited,following inclusion criteria and pre-established exclusion. All volunteers will be informed and sign a term of clarification and consent. 50 enrolled patients will receive 200 Class V dental restorations, made in four different ways, one from each experimental group, using the same universal self-etching adhesive system, which is the tested material in this study. Non-carious cervical lesions will receive the applied adhesive system in 4 different protocols separated by groups. Group Self Etching (SET) (control): no conditioning, the adhesive system will be used in 50 teeth, according to the manufacturer's instructions, in the self-etching mode. The adhesive system will be brushed during 20 seconds in the cavity, will be air-dried during 5 seconds, and activated during 10 seconds with Light Emission Diode (LED) light; Group SEE (Selective enamel etching): 37% phosphoric acid will be applied during 30 seconds, only in enamel in 50 teeth. This acid will be removed using water, the cavity will be air-dried, and then, the adhesive will be applied according to the manufacturer's instructions, as described in group SET; Group ERDry (Etch\& Rinse Dry): 37% phosphoric acid will be applied during 30 seconds, only in enamel and during 15 seconds only in dentin, in 50 teeth. This acid will be removed using water, the cavity will be air-dried, keeping dentin dry, and then, the adhesive will be applied according to the manufacturer's instructions, as described in group SET; Group ERWet (Etch\& Rinse Wet): 37% phosphoric acid will be applied during 30 seconds, only in enamel and during 15 seconds only in dentin, in 50 teeth. This acid will be removed using water, the cavity will be air-dried, keeping dentin wet, and then, the adhesive will be applied according to the manufacturer's instructions, as described in group SET. After applying the adhesive, the restorations will be made with composite resin, and evaluated every 6 months for pain assessment, shape, staining or recurrent caries, using scores. To determine in which group each tooth will be enrolled, the authors will randomize the teeth.
Conditions
- Dental Restoration Failure of Marginal Integrity
Interventions
- OTHER
-
Self-Etching Application Strategy
In Group SET, the adhesive system Futurabond Universal will be used in 50 teeth, according to the manufacturer's instructions, in the self-etching mode. The adhesive system will be brushed during 20 seconds in the cavity, will be air-dried during 5 seconds, and activated during 10 seconds with LED light; After applying the adhesive, the restorations will be made with composite Admira Fusion (VOCO GmbH, Germany), and evaluated every 6 months for pain assessment, shape, staining or recurrent caries, using scores.
- OTHER
-
Enamel Etching Application Strategy
In Group SEE, 37% phosphoric acid will be applied during 30 seconds, only in enamel in 50 teeth. This acid will be removed using water, the cavity will be air-dried, and then, the adhesive system Futurabond Universal will be used in 50 teeth, according to the manufacturer's instructions. The adhesive system will be brushed during 20 seconds in the cavity, will be air-dried during 5 seconds, and activated during 10 seconds with LED light; After applying the adhesive, the restorations will be made with composite Admira Fusion (VOCO GmbH, Germany), and evaluated every 6 months for pain assessment, shape, staining or recurrent caries, using scores.
- OTHER
-
Etch&Rinse Dry Application Strategy
In Group ERDry, 37% phosphoric acid will be applied during 30 seconds, only in enamel, and 15 seconds, only in dentin, in 50 teeth. This acid will be removed using water, the cavity will be air-dried, keeping dentin dry (but not overdry) and then, the adhesive system Futurabond Universal will be used in 50 teeth, according to the manufacturer's instructions. The adhesive system will be brushed during 20 seconds in the cavity, will be air-dried during 5 seconds, and activated during 10 seconds with LED light; After applying the adhesive, the restorations will be made with composite Admira Fusion (VOCO GmbH, Germany), and evaluated every 6 months for pain assessment, shape, staining or recurrent caries, using scores.
- OTHER
-
Etch&Rinse Wet Application Strategy
In Group ERWet, 37% phosphoric acid will be applied during 30 seconds, only in enamel, and 15 seconds, only in dentin, in 50 teeth. This acid will be removed using water, the cavity will be air-dried, keeping dentin wet and then, the adhesive system Futurabond Universal will be used in 50 teeth, according to the manufacturer's instructions. The adhesive system will be brushed during 20 seconds in the cavity, will be air-dried during 5 seconds, and activated during 10 seconds with LED light; After applying the adhesive, the restorations will be made with composite Admira Fusion (VOCO GmbH, Germany), and evaluated every 6 months for pain assessment, shape, staining or recurrent caries, using scores.
Sponsors & Collaborators
-
Universidade Estadual de Ponta Grossa
collaborator OTHER -
Universidade Federal Fluminense
lead OTHER
Principal Investigators
-
MARCOS O BARCELEIRO, DDS, PhD · Universidade Federal Fluminense
-
ALESSANDRO D LOGUERCIO, DDS, PhD · Universidade Estadual de Ponta Grossa
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- DOUBLE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Max Age
- 70 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2016-09-03
- Primary Completion
- 2017-05-31
- Completion
- 2026-11-30
Countries
- Brazil
Study Locations
More Related Trials
-
Clinical Performance of Fiber Reinforced FRC Base and Bonded CAD/CAM Resin Composite Endocrowns
NCT06348979 ·Status: COMPLETED ·Phase: NA
-
A Comparative Analysis of Biomaterials for Retrograde Filling in Apical Surgery.
NCT07246512 ·Status: ACTIVE_NOT_RECRUITING ·Phase: NA
-
Primary Molars Restorations With Encapsulated or Hand-Mixed Glass Ionomer: Clinical Trial
NCT02274142 ·Status: COMPLETED ·Phase: NA
-
Indirect Resin Composite Inlays Cemented With a Self-adhesive, Self-etch or a Conventional Resin Cement
NCT04848987 ·Status: COMPLETED ·Phase: NA
-
Influence of Resin Cement Composition on the Longevity of Intraradicular Post of Endodontically Treated Teeth
NCT03491527 ·Status: UNKNOWN ·Phase: NA
-
Influence of Temporary Filling Material Composition on the Success Rate of Endodontic Treatments
NCT03488316 ·Status: UNKNOWN ·Phase: NA
-
Clinical Performance of Milled Resin Composite in Restoration of Endodontically Treated Posterior Teeth Over One Year
NCT04518371 ·Status: COMPLETED ·Phase: NA
-
Clinical Evaluation of Self- Adhesive Bulk-fill Resin Composite Versus Conventionally Bonded Bulk-fill Resin Composite in Restoration of Proximal Lesions
NCT04888676 ·Status: UNKNOWN ·Phase: NA
-
Clinical Performance of Short Fiber Reinforced Resin Composite Versus Indirect Nanohybrid Resin Composite Onlay Restorations.
NCT03283280 ·Status: COMPLETED ·Phase: NA
-
Clinical Assessment of Preheated Versus Conventional Bulk Fill Resin Composite
NCT04152460 ·Status: UNKNOWN ·Phase: NA
-
Clinical Performance of Two Different Restorative Materials in Restoring Class II Cavities of Primary Molars
NCT06000085 ·Status: UNKNOWN ·Phase: NA
-
Indirect Pulp Capping With Resin Modified Glass Ionomer
NCT02494193 ·Status: COMPLETED ·Phase: NA
-
Assessment of I-PRF Versus Nano MTA Combined with I-PRF Scaffold in Vital Pulp Therapy in Mature Mandibular First Molars
NCT06640205 ·Status: RECRUITING ·Phase: NA
-
Clinical Performance of Fiber Reinforced FRC Base and Bonded CAD/CAM Resin Composite Endocrowns Versus Conventional Lithium Disilicate Endocrowns in Posterior Teeth (1y Randomized Clinical Trial).
NCT05337358 ·Status: UNKNOWN ·Phase: NA
-
Performance Of Cervical Restorations Using Nitric Acid and Mineral Enriched Adhesive Versus Phosphoric Acid and Universal Adhesive
NCT05928533 ·Status: COMPLETED ·Phase: NA
-
Evaluation of the Solvent Evaporation Time of Universal Adhesives in the Quality of Cervical Lesions Restorations
NCT05945173 ·Status: COMPLETED ·Phase: NA
-
Treatment of Deep Carious Lesions With Selective Caries Removal, Partial or Full Pulpotomy
NCT04807244 ·Status: UNKNOWN ·Phase: NA
-
Cost-efficacy of Atraumatic Restorations (ART) Using Different Encapsulated Glass Ionomer Cement
NCT02730000 ·Status: COMPLETED ·Phase: NA
-
Clinical Efficacy of Ceramic vs Resin Block Endocrown
NCT04033380 ·Status: UNKNOWN ·Phase: NA
-
Endocrowns vs.Ceramic Onlays Used in Endodontically Treated Teeth- Randomized Clinical Study
NCT03064516 ·Status: COMPLETED ·Phase: NA
-
Clinical Evaluation of a Universal Adhesive in Noncarious Cervical Lesions
NCT02172664 ·Status: COMPLETED ·Phase: NA
-
Clinical and Radiographic Evaluation of Bioceramic Putty MTA Versus MTA in Pulpotomy of Immature Permanent Molars
NCT06219824 ·Status: NOT_YET_RECRUITING ·Phase: PHASE3
-
Clinical and Radiographic Outcomes of Partial Pulpotomy Procedure in Primary Molars Utilizing Different Capping Materials and Different Restorative Methods
NCT06227390 ·Status: COMPLETED ·Phase: NA
-
Clinical Evaluation of Bioactive Restorative Materials
NCT07003360 ·Status: ACTIVE_NOT_RECRUITING ·Phase: NA
-
Clinical Performance of Injection-Molding Vs. Incremental Packing of Resin Composite in Cavitated Posterior Teeth
NCT05020093 ·Status: UNKNOWN ·Phase: NA