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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT05766696
Other study ID # DeltaART
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date May 2023
Est. completion date May 2025

Study information

Verified date March 2023
Source DMG Dental Material Gesellschaft mbH
Contact Faheema Kimmie-Dhansay
Phone +2721 9373152
Email fkimmie@uwc.ac.za
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study will investigate the performance and cost-effectiveness of glass-ionomer restorations placed in school children in an outreach setting in rural areas in South Africa over a 2-year period, when placed using either ART (in a classroom) or conventional (in a mobile clinic) cavity preparation.


Description:

Access to dental care in South African townships is very limited, as indicated by a caries prevalence of 84% and severity of 4.9 (dmft) in 6 year olds. To tackle this burden school-based tooth-brushing programs have been suggested to be cost-effective while reducing inequalities in accessibility. However, despite their efforts, the caries burden remains high. Alternatives are mobile dental services or treatment techniques that do not require extensive equipment such as Atraumatic Restorative Treatment (ART). Mobile dental services are more cost-effective than stationary clinics, but the costs of acquiring, outfitting, and running a mobile dental truck are factors that may hamper the broader use of this model. ART on the other hand is easy to execute with minimal equipment and monetary resources. But the drawback is a typically lower survival rate of ART restorations compared to conventional placed restorations. This study aims to further assess and compare the performance and cost-effectiveness of glass-ionomer restorations when placed using either ART (in a classroom) or conventional (in a mobile clinic) cavity preparation in South African school children stemming from a periurban area. The results of this research may help to assess and implement future oral health care programs.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 200
Est. completion date May 2025
Est. primary completion date May 2025
Accepts healthy volunteers No
Gender All
Age group 4 Years to 8 Years
Eligibility General Inclusion Criteria: - Children (4-8 years of age) - Guardians have given informed consent - Child is cooperative and assented Inclusion criteria for teeth - Cavity > 1 mm - Tooth has no pathological mobility - Tooth has no preexisting developmental defects - Tooth has no pulp exposure or is indication for endodontic treatment - No pain, fistula or abscess related to the selected tooth Exclusion criteria for teeth - Cavity > 1 mm - Tooth has no pathological mobility

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Atraumatic Restorative Treatment (ART)
Conventional glass-ionomer restorations are placed using the Atraumatic Restorative Treatment (ART) technique. Essentially, cavities are prepared using hand instrument excavators. Afterwards, the cavity is conditioned (using a 10% polyacrylic acid conditioner) and cleaned, with subsequent insertion of a conventional restorative glass-ionomer. During the curing phase, Vaseline will be applied to all restoration surfaces for moisture protection. The treatment will be conducted in a class room. As concomitant treatment, all participants will receive supervised toothbrushing during the study using 1,450 ppm fluoride toothpaste once a day.
Conventional Cavity Preparation
Conventional glass-ionomer restorations are placed after conventional cavity preparation. Essentially, cavities are prepared using rotary instruments/diamond burs. Afterwards, the cavity is conditioned (using a 10% polyacrylic acid conditioner) and cleaned, with subsequent insertion of a conventional restorative glass-ionomer. During the curing phase, Vaseline will be applied to all restoration surfaces for moisture protection. The treatment will be conducted in a mobile clinic. As concomitant treatment, all participants will receive supervised toothbrushing during the study using 1,450 ppm fluoride toothpaste once a day.

Locations

Country Name City State
South Africa Nyameko and Itsitsa Primary Schools Mfuleni Western Cape

Sponsors (1)

Lead Sponsor Collaborator
DMG Dental Material Gesellschaft mbH

Country where clinical trial is conducted

South Africa, 

Outcome

Type Measure Description Time frame Safety issue
Other Lesion size Lesion size (<3.5mm; 3.5mm-5.5mm; >5.5mm) will be recorded to evaluate the impact of lesion size on survival rate Intervention at baseline
Other Treatment time (continuous outcome, minutes) Treatment time (from lifting intrument to placing instrument) for each restoration will be recorded using a stopwatch Intervention at baseline
Primary Survival rate of posterior occlusal multi-surface restorations Restorations are assessed using the ART criteria by Frencken:
Survival: Code 0 (Present, satisfactory); Code 1 (Present, slight deficiency at cavity margin of less than 0.5 mm)
Failure: Code 2 (Present, deficiency at cavity margin of 0.5 mm or more); Code 3 (Present, fracture in restoration); Code 4 (Present, fracture in tooth); Code 5 (Present, overextension of approximal margin of 0.5 mm or more); Code 6 (Not present, most or all of restoration missing); Code 7 (Not present, other restorative treatment performed); Code C (Dentin carious lesion present)
24 months
Secondary Survival rate of restorations depending on lesion type (occlusal single surface, occlusal multi surface and approximal restorations) Restorations are divided in the subgroups "occlusal single surface", "occlusal multi surface" and "approximal restorations" and restorations are assessed using the ART criteria by Frencken:
Survival: Code 0 (Present, satisfactory); Code 1 (Present, slight deficiency at cavity margin of less than 0.5 mm)
Failure: Code 2 (Present, deficiency at cavity margin of 0.5 mm or more); Code 3 (Present, fracture in restoration); Code 4 (Present, fracture in tooth); Code 5 (Present, overextension of approximal margin of 0.5 mm or more); Code 6 (Not present, most or all of restoration missing); Code 7 (Not present, other restorative treatment performed); Code C (Dentin carious lesion present)
6, 12 and 24 months
Secondary Incremental cost-effectiveness ratio (ICER) Incremental cost-effectiveness ratio will be calculated as "difference in costs of failures / difference in failures" to assess "cost/ savings per failure prevented".
For costing, a payers perspective will be assumed and costing will be calculated on a "per restoration" basis. For this material, transport, personnel and equippment costs will be assessed. All materials used in each procedure will have their specifications and quantity registered. Capital costs will be annualized and the proportion of time it took to complete the intervention will be calculated and applied to the annualized capital costs to estimate the cost per restoration. Prices will be inferences from the market value converted in US Dollars and obtained by the medium of the values from different places that commercialized the referred products.
6, 12 and 24 months
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