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HEMA-free Universal Adhesives for Restoring Non-carious Cervical Lesions

Cairo University (CU) logo

Cairo University (CU)

Status

Not yet enrolling

Conditions

Universal Adhesive

Treatments

Other: Acetone based HEMA -free universal Adhesive
Other: Isopropanol based HEMA- free universal Adhesive

Study type

Interventional

Funder types

Other

Identifiers

NCT05497583
universal adhesive

Details and patient eligibility

About

because of the recent introduction of universal adhesives, little information is currently available about the bond durability of universal adhesives to various substrates. Evaluation of bond durability is important since the stability of the bond between the adhesive and substrates is related to the clinical success of restorations. Because significant hydrolysis of the dentin-resin interface occurs after 6-12 months, a clinical trial of at least 18 months' duration is indicated to more accurately depict the likelihood of long-term clinical success

Full description

Cervical restorations are ever challenging because of difficulties in moisture control, caries access, and proximity to the gingival margin. Both mechanical and non-mechanical factors act to hinder the longevity of cervical restoration newer materials are readily introduced in the market with improved chemomechanical properties, longevity, patient safety, and comfort.

The introduction of new-generation adhesive systems has aimed at reducing technique sensitivity and the number of clinical steps required for adhesion. There has been a trend toward the use of less time-consuming options, continuing this trend, universal adhesives have recently been introduced to the profession. However, because of the recent introduction of universal adhesives, little information is currently available about the bond durability of universal adhesives to various substrates. Evaluation of bond durability is important since the stability of the bond between the adhesive and substrates is related to the clinical success of restorations. Although the most reliable conclusions about the performance of adhesives in the oral environment are derived from clinical trials.

To evaluate the effectiveness and clinical performance of adhesive systems, the American Dental Association (ADA) recommends clinical trials on non-carious cervical lesions (NCCLs), as composite resin restorations only remain bonded to these lesions by the micromechanical interlocking produced by the adhesive systems. The immediate, short-term, and long-term bonding performance of adhesive systems are then evaluated by retention, marginal integrity, and marginal discoloration. There are many attempts to improve bonding to substrates, bond strength, and bond durability, one of these attempts is the newly introduced universal adhesive (BeautiBond ).

Enrollment

28 estimated patients

Sex

All

Ages

18 to 60 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Participants had to be in good general health, be at least 18 years old
  • have an acceptable oral hygiene level
  • Participants were required to have NCCLs in different teeth preferably anterior or posterior that needed to be restored.
  • These lesions had to be noncarious
  • deeper than 1 mm
  • involve both the enamel and dentin of vital teeth without mobility.

Exclusion criteria

  • Uncooperative behavior, limits the use of adhesive due to hampering of adequate field or isolation techniques throughout the procedure.
  • Patients allergic to the adhesive material. Patients with extremely poor oral hygiene
  • severe or chronic periodontitis
  • heavy bruxism habits
  • Pulp involvement

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

28 participants in 2 patient groups

Acetone based HEMA free Universal Adhesive
Experimental group
Description:
Patients with non-carious cervical lesions will be treated with Acetone Based HEMA-free Universal Adhesive (BeautiBond universal adhesive ) applied in a self-etch approach with (SE) selective enamel etching.
Treatment:
Other: Acetone based HEMA -free universal Adhesive
Isopropanol based HEMA-free universal Adhesive
Active Comparator group
Description:
Patients with non-carious cervical lesions will be treated with isopropanol-based HEMA-free universal Adhesive (Prime\&Bond universal™ Adhesive system) applied in a self-etch approach with (SE) selective enamel etching.
Treatment:
Other: Isopropanol based HEMA- free universal Adhesive

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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