Clinical Evaluation of Dimethyl Sulfoxide Wet Bonding Technique

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

NOT_YET_RECRUITING

Clinical Phase

NA

Total Enrollment

68 participants

Study Classification

INTERVENTIONAL

Study Start Date

2024-10-20

Study Completion Date

2025-04-01

Brief Summary

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Dimethyl sulfoxide (DMSO) wet bonding has shown promising results in several in vitro studies. However, there are a lack of clinical trials which prove the advantages of this technique. The aim of the study is to clinically assess the effect of DMSO wet bonding on composite restoration in non carious cervical lesions.

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Detailed Description

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Conditions

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Dimethyl Sulfoxide

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

FACTORIAL

Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Participants Investigators

Study Groups

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Universal single bond adhesive

Group Type ACTIVE_COMPARATOR

Universal single bond adhesive

Intervention Type OTHER

Will be applied and light cured for 20 seconds.

DMSO application before Universal single bond adhesive

Group Type EXPERIMENTAL

Universal single bond adhesive

Intervention Type OTHER

Will be applied and light cured for 20 seconds.

DMSO

Intervention Type OTHER

DMSO application on tooth followed by active application of universal single bond adhesive and light cured for 20 seconds.

Interventions

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Universal single bond adhesive

Will be applied and light cured for 20 seconds.

Intervention Type OTHER

DMSO

DMSO application on tooth followed by active application of universal single bond adhesive and light cured for 20 seconds.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Two similar non carious cervical lesions (NCCLs) on the facial/labial surfaces of premolars.
* NCCLs of score 1-3 on the Smith and Knight tooth wear index.
* Favorable occlusion and teeth are in normal contact.

Exclusion Criteria

* NCCLs on the lingual surface.
* Medically compromised individuals.
* Periodontally compromised teeth.
* Bruxism and visible wear facets in the posterior dentition.
* Fractured or visibly cracked premolars and canines.
* Known allergies to resin-based restorative materials.
* Presently undergoing orthodontic treatment.
* Abutment teeth for fixed or removable prostheses.

Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No