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Pre-etching of Dentin Before Restorations With High Viscosity Glass Ionomer Cement (CEPECO4)

Primary Purpose

Dental Caries

Status
Withdrawn
Phase
Not Applicable
Locations
Brazil
Study Type
Interventional
Intervention
HVGIC restoration with pre-etching
HVGIC restoration with non pre-etching
Sponsored by
Universidade Ibirapuera
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Dental Caries

Eligibility Criteria

4 Years - 8 Years (Child)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Patients with carious lesion of occlusoproximais in primary molars

Exclusion Criteria:

  • Patients will be excluded with special needs, using orthodontics devices and/or systemic diseases which may affect the oral cavity.
  • Also, teeth with pulp exposure, spontaneous pain, mobility, presence of abscess or fistula next to the tooth, teeth with restorations, sealants or enamel formation defects will also be excluded.

Sites / Locations

  • Tamara Kerber Tedesco

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

HVGIC restoration with pre-etching

HVGIC restoration with non pre-etching

Arm Description

Pre-etching of the surface with polyacrylic acid for 10 s, followed by HVGIC restoration.

HVGIC restoration without the pre-etching of the surface.

Outcomes

Primary Outcome Measures

Survival of restorations
Comparing the survival of HVGIC restorations without pre-etching with HVGIC restorations with pre-etching by clinical assessment using a criteria proposed by Roleveld et al., 2006.

Secondary Outcome Measures

Caries lesion progression will be evaluated by comaparison of radiograph immediately after the restoration
The caries lesion progression will be evaluated by comaparison of radiograph immediately after the restoration and after 24 months.
Cost-efficacy
The duration of the treatments (time of treatment) and the cost of the materials used will be considered for the estimation of the cost-efficacy of the treatments by a ratio - cost/efficacy, being efficacy considered the tooth survival.
Discomfort regarding the treatment options by a Wong-Baker FACES pain rating scale
Children-reported discomfort regarding the treatment options by a Wong-Baker FACES pain rating scale. The scale present 6 different faces since "very happy" until "very sad" with the treatment.

Full Information

First Posted
December 18, 2018
Last Updated
May 30, 2022
Sponsor
Universidade Ibirapuera
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1. Study Identification

Unique Protocol Identification Number
NCT03785769
Brief Title
Pre-etching of Dentin Before Restorations With High Viscosity Glass Ionomer Cement
Acronym
CEPECO4
Official Title
Effect of Pre-etching of Dentin on Survival of Restorations With High Viscosity Glass Ionomer Cement in the Atraumatic Restorative Treatment - Randomized Clinical Trial Restorations With High Viscosity Glass Ionomer Cement
Study Type
Interventional

2. Study Status

Record Verification Date
May 2022
Overall Recruitment Status
Withdrawn
Why Stopped
The Outbreak of COVID-19.
Study Start Date
January 1, 2022 (Anticipated)
Primary Completion Date
December 1, 2022 (Anticipated)
Study Completion Date
December 1, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Universidade Ibirapuera

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
The objective of this randomized clinical trial is to evaluate the survival of restoration with high viscosity glass ionomer cement (HVGIC) with pre-etching with polyacrilic acid compared with no pre-etching in order to treat occlusoproximais caries lesion in primary molars, as well as the impact of those treatments in the caries lesion progression, the cost-efficacy of the procedures and the discomfort reported by the patient. Children of 4 to 8 years will be selected in the Pediatric Dentistry Clinic of Universidade Ibirapuera. 192 teeth will be randomized in 2 experimental groups: (1) HVGIC restoration with pre-etching and (2) HVGIC restoration with no pre-etching. Will be considered as primary outcome the survival of the restoration evaluated after 6, 12, and 24 months by two trained examiners. The carious lesions progression will be evaluated after 24 months of follow-up. The time of the treatments and the cost of the materials will be considered to estimate the cost-efficacy of each treatment. The discomfort reported by the participant will be measured after each procedure following the Wong-Baker scale. For the primary outcome, Kaplan-Meier survival and the Long-Rank test will be used in order to compare the two groups. Cox regression will be performed in order to evaluate thee influence of explanatory variables on the outcome.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Dental Caries

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantOutcomes Assessor
Masking Description
Double-blind (Patient and Examiner) will not be able to blinding the operator due to the obvious difference between the techniques
Allocation
Randomized
Enrollment
0 (Actual)

8. Arms, Groups, and Interventions

Arm Title
HVGIC restoration with pre-etching
Arm Type
Active Comparator
Arm Description
Pre-etching of the surface with polyacrylic acid for 10 s, followed by HVGIC restoration.
Arm Title
HVGIC restoration with non pre-etching
Arm Type
Experimental
Arm Description
HVGIC restoration without the pre-etching of the surface.
Intervention Type
Procedure
Intervention Name(s)
HVGIC restoration with pre-etching
Intervention Description
Pre-etching of the surface with polyacrylic acid for 10 s, followed by washing and drying the cavity with cotton balls; and fill with HVGIC, inserted into the cavity with the aid of an insertion spatula and adapted to the cavity by the digital pressure technique.
Intervention Type
Procedure
Intervention Name(s)
HVGIC restoration with non pre-etching
Intervention Description
Restoration with HVGIC, inserted into the cavity with the aid of an insertion spatula and adapted to the cavity by the digital pressure technique.
Primary Outcome Measure Information:
Title
Survival of restorations
Description
Comparing the survival of HVGIC restorations without pre-etching with HVGIC restorations with pre-etching by clinical assessment using a criteria proposed by Roleveld et al., 2006.
Time Frame
24 months
Secondary Outcome Measure Information:
Title
Caries lesion progression will be evaluated by comaparison of radiograph immediately after the restoration
Description
The caries lesion progression will be evaluated by comaparison of radiograph immediately after the restoration and after 24 months.
Time Frame
Immediately after the restoration and 24 months
Title
Cost-efficacy
Description
The duration of the treatments (time of treatment) and the cost of the materials used will be considered for the estimation of the cost-efficacy of the treatments by a ratio - cost/efficacy, being efficacy considered the tooth survival.
Time Frame
24 months.
Title
Discomfort regarding the treatment options by a Wong-Baker FACES pain rating scale
Description
Children-reported discomfort regarding the treatment options by a Wong-Baker FACES pain rating scale. The scale present 6 different faces since "very happy" until "very sad" with the treatment.
Time Frame
Immediately after the treatment

10. Eligibility

Sex
All
Minimum Age & Unit of Time
4 Years
Maximum Age & Unit of Time
8 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Patients with carious lesion of occlusoproximais in primary molars Exclusion Criteria: Patients will be excluded with special needs, using orthodontics devices and/or systemic diseases which may affect the oral cavity. Also, teeth with pulp exposure, spontaneous pain, mobility, presence of abscess or fistula next to the tooth, teeth with restorations, sealants or enamel formation defects will also be excluded.
Facility Information:
Facility Name
Tamara Kerber Tedesco
City
São Paulo
State/Province
SP
ZIP/Postal Code
04545-000
Country
Brazil

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
Individual participant data will be available on Mendeley database.

Learn more about this trial

Pre-etching of Dentin Before Restorations With High Viscosity Glass Ionomer Cement

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