NCT05635981

Brief Summary

In restorative dentistry, to enhance bond strength between dentin and simplified adhesive systems, new materials or applications are constantly being developed all the time. In order to create a better hybrid layer quality, modifications are made to the chemical contents and application methods of the adhesives. For inhibition or slow down of collagen or resin matrix degradation at the adhesive interface, procedures like using protease enzyme inhibitors or additional hydrophobic layer applications are tested by in vitro and in vivo studies. The main goal of this double-blind randomized clinical trial is to evaluate the 18-month clinical performances of two different one-step dentin adhesives that were applied alone or with an additional hydrophobic adhesive layer to non-carious cervical lesions. The hypotheses are that (1) Additional Hydrophobic Adhesive layer application can provide better clinical performance in class V restorations and, (2) the HEMA content will cause statistically different clinical performances.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
31

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Jan 2019

Typical duration for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

January 20, 2019

Completed
2.1 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 10, 2021

Completed
22 days until next milestone

Study Completion

Last participant's last visit for all outcomes

April 1, 2021

Completed
1.6 years until next milestone

First Submitted

Initial submission to the registry

October 28, 2022

Completed
1 month until next milestone

First Posted

Study publicly available on registry

December 2, 2022

Completed
Last Updated

December 2, 2022

Status Verified

November 1, 2022

Enrollment Period

2.1 years

First QC Date

October 28, 2022

Last Update Submit

November 22, 2022

Conditions

Keywords

Non Carious Cervical LesionAdditional Adhesive Layer ApplicationFDI CriteriaClass V RestorationsSplit-Mouth Clinical Study

Outcome Measures

Primary Outcomes (9)

  • Fracture and Retention

    While scoring the fracture and retention parameters, restoration; If there is no fracture with a score of 1 if there are linear cracks with a score of 2 if there are large cracks and fractures that do not affect the marginal integrity and contact with a score of 3 if there are small fractures affecting the marginal integrity or contact or if there are fractures less than half the size of the restoration a score of 4 is a large part of the restoration or In case of losing all, it is evaluated with a score of 5.

    18 month

  • Surface Luster

    Restoration; A score of 1 if the surface's glossiness is at the same level as enamel, a score of 2 if there are opacity and pores that cannot be noticed from the speaking distance, an acceptable opacity when covered with saliva, or a score of 3 if more than 1/3 of the surface has pores, and a score of 4 if there is a roughness that cannot be masked with saliva and cannot be removed by polishing. If there is a roughness that causes plaque retention, it is evaluated with a score of 5.

    18 month

  • Marginal Staining

    It is scored as 1 if there is no discoloration on the marginal edges, 2 if there is discoloration that can be easily removed by polishing, 3 if there is moderate discoloration that cannot be accepted aesthetically, 4 if there is noticeable large discoloration that requires repair, and 5 if there is deep marginal discoloration that cannot be repaired.

    18 month

  • Marginal Adaptation

    If there is no gap at the marginal margins and the tooth tissue is compatible 1, if there is a small gap, line, fracture or step that can be removed by polishing, 2 if there are indentations, if there is a small gap that cannot be removed by polishing, if there is more than one marginal fracture or large indentations 3, if the dentin is exposed repair It is scored 4 if there are large openings, fractures, or indentations that require it, and 5 if there are large openings and irregularities where part of the restoration is lost.

    18 month

  • Color Match and Translucency

    While scoring the color match and translucency, the restoration and the tissue color are compatible with each other and there is no difference in translucency 1, if there are minor changes in color or translucency 2, if there is a clear but acceptable color difference (more opaque-translucent-light-dark) 3, at a level that can be corrected with repair and 4 if there is a significant color difference, and 5 if there is an unacceptable color difference.

    18 month

  • Esthetic Anatomical Form

    While scoring the aesthetic anatomical form, the form of the restoration is scored 1 if it is ideal, 2 if it is not ideal but will be ideal with a small intervention, 3 if it is not ideal but aesthetically acceptable, 4 if it is not aesthetically acceptable and repair is required, and 5 if it is unacceptable and needs to be changed.

    18 month

  • Periodontal Response

    During periodontal response scoring, if there is no plaque accumulation, pocket formation or inflammation in the restored tooth, 1, if there is a small amount of plaque accumulation and no inflammation and pocket formation, 2, if the papillary bleeding index increases by 1 point compared to the baseline, 3 if the papillary bleeding index increases by more than 1 point and periodontal bleeding index increases by more than 1 point It is scored 4 if there is an increase in the pocket more than 1 mm, and 5 if there is acute gingivitis or acute periodontitis.

    18 month

  • Post Operative Sensitivity

    Restoration; It is evaluated with a score of 1 if there is no sensitivity complaint, with a score of 2 if there is a small amount of sensitivity for a short time, and a score of 3 if the patient has no complaints and moderate sensitivity, with a score of 3 if there is hypersensitivity that does not require restoration replacement but requires repair, and a score of 4 if endodontic treatment is required.

    18 month

  • Secondary Caries

    Restoration; It is evaluated with a score of 1 if there is no caries formation, with a score of 2 if there is small and localized demineralization, and a score of 3 if there is demineralization in a large area that requires only precautions, and a score of 4 if there is cavitation that requires repair, and a score of 5 if there is a deep caries that cannot be repaired.

    18 month

Study Arms (4)

Clearfil S3 Bond Plus

ACTIVE COMPARATOR

After selective etching is applied to the enamel surface, Clearfil S3 Bond Plus is applied according to the manufacturer's instructions, restorations are completed with Clearfil Majesty ES-2. Clearfil S3 Bond Plus: one-step self-etch adhesive with HEMA

Other: Clearfil Majesty ES-2 Resin Composit Application to Non-carious Cervical Lesions

Clearfil S3 Bond Plus with Additional Hydrophobic Adhesive Layer Application

EXPERIMENTAL

After selective etching is applied to the enamel surface, Clearfil S3 Bond Plus is applied according to the manufacturer's instructions. Heliobond is applied as an additional hydrophobic adhesive layer and restorations are completed with Clearfil Majesty ES-2. Clearfil S3 Bond Plus: one-step self-etch adhesive with HEMA Heliobond: hydrophobic adhesive with Bis-GMA and TEGDMA

Other: Clearfil Majesty ES-2 Resin Composit Application to Non-carious Cervical Lesions

G-Premio Bond

ACTIVE COMPARATOR

After selective etching is applied to the enamel surface, G-Premio Bond is applied according to the manufacturer's instructions, restorations are completed with Clearfil Majesty ES-2. G-Premio Bond: universal adhesive without HEMA

Other: Clearfil Majesty ES-2 Resin Composit Application to Non-carious Cervical Lesions

G-Premio Bond with Additional Hydrophobic Adhesive Layer Application

EXPERIMENTAL

After selective etching is applied to the enamel surface, G-Premio Bond is applied according to the manufacturer's instructions. Heliobond is applied as an additional hydrophobic adhesive layer and restorations are completed with Clearfil Majesty ES-2. G-Premio Bond: universal adhesive without HEMA Heliobond: hydrophobic adhesive with Bis-GMA and TEGDMA

Other: Clearfil Majesty ES-2 Resin Composit Application to Non-carious Cervical Lesions

Interventions

A restorative treatment method that is applied to non-carious cervical lesions using composite resin restoration after adhesive material application.

Clearfil S3 Bond PlusClearfil S3 Bond Plus with Additional Hydrophobic Adhesive Layer ApplicationG-Premio BondG-Premio Bond with Additional Hydrophobic Adhesive Layer Application

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • and over 18 years old
  • Having acceptable oral hygiene
  • Good general health
  • Having at least 20 teeth in occlusion
  • Presence of at least 4 non-carious cervical lesions in the mouth that require treatment
  • Lesions without caries
  • Patient's consent to come to control appointments
  • Vital and non-mobility of the tooth with the lesion
  • During occlusion, the tooth with the lesion is in contact with the antagonist tooth.

You may not qualify if:

  • Under 18 years old
  • Having poor oral hygiene
  • Poor general health condition
  • Pregnancy or breastfeeding status
  • Orthodontic application in the last 3 months
  • The tooth with the lesion has pulpitis, mobility or it is non-vital
  • Presence of advanced bruxism
  • The tooth with the lesion is a prosthetic abutment
  • Presence of advanced periodontitis or periodontal surgery in the last 3 months

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Istanbul University

Istanbul, Fatih, Turkey (Türkiye)

Location

Study Officials

  • Meriç Berkman, pHD

    Istanbul University

    PRINCIPAL INVESTIGATOR
  • Safa Tuncer, Professor

    Istanbul University

    STUDY CHAIR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
DOUBLE
Who Masked
PARTICIPANT, OUTCOMES ASSESSOR
Masking Details
The operator who performed the composite restorations is not blinded. Two evaluators who are responsible for the assessment of the clinical performance of restorations according to FDI criteria and the participants are blinded to the study groups.
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal Investigator

Study Record Dates

First Submitted

October 28, 2022

First Posted

December 2, 2022

Study Start

January 20, 2019

Primary Completion

March 10, 2021

Study Completion

April 1, 2021

Last Updated

December 2, 2022

Record last verified: 2022-11

Data Sharing

IPD Sharing
Will share
Shared Documents
STUDY PROTOCOL, SAP, ICF, CSR, ANALYTIC CODE

Locations