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Evaluation of restorations performed with two glass ionomer cements on temporary teeth.

Randomized clinical trial of two high viscosity´s restorative Glass Ionomer Cements used in deciduous molars.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-5jx29r
Enrollment
Unknown
Registered
2017-09-19
Start date
2016-03-01
Completion date
Unknown
Last updated
2025-10-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Dental Caries and Stomatognathic System Abnormalities.

Interventions

Group 1 - Technique of the Atraumatic Removal of carious tissue (ART) and restoration with Cement of Modified Experimental Glass - IONZ® - FGM - Number of participants: 21 children in the age group b
Procedure/surgery

Sponsors

Universidade Metropolitana de Santos (UNIMES)
Lead Sponsor
Universidade Metropolitana de Santos (UNIMES)
Collaborator

Eligibility

Age
5 Years to 8 Years

Inclusion criteria

Inclusion criteria: Healthy child from 05 to 08 years old, without systemic alteration; good behavior; Presenting clinically at least two deciduous molars with dentin caries lesion involving only the occlusal, with direct vision and access, without clinical and radiographic signs and symptoms of pulp involvement.

Exclusion criteria

Exclusion criteria: Child with systemic impairment. Non-contributory behavior. Black, Class II, III or IV type carious lesion. Clinically: carious lesion involving enamel, deficient restorations, small carious lesions in dentin (no access for hand excavators), occult caries lesions, sign and / or clinical symptom of pulp involvement, clinical impossibility of restoration. Radiographically: evidence of pulp involvement, carious lesion extending beyond 2/3 of the dentin.

Design outcomes

Primary

MeasureTime frame
The expected outcome is the effectiveness of the restorations, which will be measured by evaluating the longevity of the restorations in the 03, 06 and 12 month periods and considered as "Clinical Success" the restorations that fit the scores 0 (Present, without defect) 1 ( Present, small defects in the margin less than 0.5 mm deep, no need for repair) and 7 (Present, surface wear less than 0.5 mm, no need for replacement) based on the clinical evaluation scale of Frencken. The aforementioned scores will be obtained through clinical and radiographic monitoring during 03, 06 and 12 month intervals.

Secondary

MeasureTime frame
Secondary outcomes are not expected

Countries

Brazil

Contacts

Public ContactLara Motta

Universidade Nove de Julho

larajmotta@terra.com.br+55 11 998829511

Outcome results

None listed

Source: REBEC (via WHO ICTRP)