Comparison of Two GIC's in the Restoration of Posterior Class II Lesions in the Primary Dentition

Sponsor
DMG Dental Material Gesellschaft mbH (Industry)
Overall Status
Not yet recruiting
CT.gov ID
NCT05965297
Collaborator
University of Coimbra (Other), University Arthur Sá Earp Neto (Other)
140
2
2
84
70
0.8

Study Details

Study Description

Brief Summary

This study will investigate the clinical performance of a novel restorative glass ionomer (DeltaFil, DMG) in comparison to an established restorative glass ionomer (Riva Self Cure HV, SDI) in the restoration of Class II cavities in primary molars.

Condition or Disease Intervention/Treatment Phase
  • Device: DeltaFil
  • Device: Riva Self Cure HV
N/A

Detailed Description

Dental caries (tooth decay) remains one of the most prevalent diseases worldwide. It is a dynamic and continuous process that, if uncontrolled, eventually leads to cavitation and the need for restorative treatment to maintain the form and function of the tooth.Today there are many possibilities for direct restorations, e.g. resin composites, compomers, resin-modified glass ionomer cements (RMGICs) and glass ionomer cements (GICs), which all offer their own advantages and disadvantages.

GIC are particularly suitable for treatments in young patients due to their high biocompatibility, fluoride release, less moisture and technique sensitivity as well as compatibility with Atraumatic restorative treatment (ART) treatment. However, these materials have lower mechanical properties compared to other restorative materials, which negatively affects the survival rate when placed in load bearing areas. Fracture, loss and wear being the most common causes for failure.

This randomized, controlled non-inferiority trial aims to evaluate the performance of the new restorative glass ionomer DeltaFil, that offers an increased fracture toughness, in comparison to an established restorative glass-ionomer (Riva Self Cure HV).

Study Design

Study Type:
Interventional
Anticipated Enrollment :
140 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Noninferiority trialNoninferiority trial
Masking:
Single (Participant)
Primary Purpose:
Treatment
Official Title:
Comparison of Two Conventional Glass Ionomer Cements in the Restoration of Posterior Class II Lesion in the Primary Dentition: a Randomized Controlled Non Inferiority Trial
Anticipated Study Start Date :
Aug 1, 2023
Anticipated Primary Completion Date :
Aug 1, 2027
Anticipated Study Completion Date :
Aug 1, 2030

Arms and Interventions

Arm Intervention/Treatment
Experimental: DeltaFil

Class II restorations are placed in primary molars after conventional cavity preparation.

Device: DeltaFil
Cavities are prepared using rotary instruments/diamond burs. Afterwards, the cavity is conditioned (using DeltaFil conditioner) and cleaned, with subsequent insertion of a conventional restorative glass-ionomer (DeltaFil). During the curing phase and after finishing Riva Coat will be applied to all restoration surfaces for moisture protection.

Active Comparator: Riva Self Cure HV

Class II restorations are placed in primary molars after conventional cavity preparation.

Device: Riva Self Cure HV
Cavities are prepared using rotary instruments/diamond burs. Afterwards, the cavity is conditioned (using Riva conditioner) and cleaned, with subsequent insertion of a conventional restorative glass-ionomer (Riva Self Cure HV). During the curing phase and after finishing Riva Coat will be applied to all restoration surfaces for moisture protection.

Outcome Measures

Primary Outcome Measures

  1. Survival rate of Class II restorations [24 months]

    Restorations are clinically assessed using the Fédération Dentaire Internationale (FDI) criteria. A "surviving" restoration is defined as a restoration that is still present at the time of evaluation and has no individual FDI criteria with a score of 5 (clinically poor).

Secondary Outcome Measures

  1. Survival rate of Class II restorations [6, 12, 36, 48 and 60 months]

    Restorations are clinically assessed using the FDI criteria. A "surviving" restoration is defined as a restoration that is still present at the time of evaluation and has no individual FDI criteria with a score of 5 (clinically poor).

  2. Individual FDI parameter assessment [Baseline, 6, 12, 24, 36, 48 and 60 months]

    Restorations are clinically assessed using the FDI criteria. Specifically, the following criteria are assessed individually on a scale from 1 "very good" to 5 "clinicially poor": Esthetic properties (Surface Luster; Surface Staining; Color Match; Anatomical Form); Functional properties (Fractures and Retention; Wear; Approximal Contact Point and Contour; Patient view); Biological properties (Postoperative Hypersensitivity & Tooth Vitality; Recurrence of Caries, Erosion, Abfraction; Periodontal Response; Tooth Integrity;Adjacent mucosa)

Other Outcome Measures

  1. Caries Experience [Baseline, 6, 12, 24, 36, 48 and 60 months]

    To assess caries experience the dmft score will be recorded. dmft refers to the number of primary teeth (t) with either decay (d), missing due to caries (m) or a filling (f).

  2. Oral Hygiene [Baseline, 6, 12, 24, 36, 48 and 60 months]

    Oral hygiene will be assessed using the Oral Hygiene Index-Simplified (OHI-S).

Eligibility Criteria

Criteria

Ages Eligible for Study:
4 Years to 8 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • At least 1 and up to 3 primary molars with either International Caries Detection and Assessment System (ICDAS) lesions stage 2-5 or preexisting restorations requiring placement/replacement of Class II restorations

  • Defects limited to occlusal-proximal surface, with cavity sizes smaller than 3 mm mesio-distally and 3 mm in the occluso-cervical and bucco-lingual directions measured with a World Health Organization (WHO)-graded periodontal probe

  • Teeth should have both adjoining and their antagonist teeth present. After restoration the restored tooth should enable appropriate proximal contacts on both mesial and distal surfaces after setting of the class II restoration and be in occlusion with the antagonist tooth

  • Good access

  • Good general health (ASA I, II)

  • Good oral hygiene (OHI-S < 1.9)

  • Guardians have given informed consent

  • Child is cooperative and assented

Exclusion Criteria:
  • Known allergy/ sensitivity to GIC or other materials used in this study

  • Space maintainers or orthodontic appliances

  • Tooth has a caries lesion or restoration other than those included in the study

  • Tooth has pathological mobility

  • Tooth has preexisting developmental defects

  • Tooth with pulp exposure or indication for endodontic treatment

  • Pain, fistula or abscess related to the selected tooth

  • Obvious signs of parafunctional habits (e.g. bruxism)

  • Participation in another study

  • Incapable to participate in the recall visits at the university hospital

Contacts and Locations

Locations

Site City State Country Postal Code
1 University Arthur Sá Earp Neto, Dental School - Pediatric Dentistry Clinic Petrópolis Brazil
2 University of Coimbra, Faculty of Medicine, Paediatric and Preventive Dentistry Institute Coimbra Portugal

Sponsors and Collaborators

  • DMG Dental Material Gesellschaft mbH
  • University of Coimbra
  • University Arthur Sá Earp Neto

Investigators

  • Study Chair: Susanne Effenberger, Dr., DMG Dental Material Gesellschaft mbH

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
DMG Dental Material Gesellschaft mbH
ClinicalTrials.gov Identifier:
NCT05965297
Other Study ID Numbers:
  • DeltaFill
First Posted:
Jul 28, 2023
Last Update Posted:
Jul 28, 2023
Last Verified:
Jul 1, 2023
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by DMG Dental Material Gesellschaft mbH
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jul 28, 2023