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Comparison of Conventional Versus Conservative Caries Removal in Primary Teeth (Caries_removal)

Primary Purpose

Dental Caries Extending Into Dentin

Status
Unknown status
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Carious dentin removal
Sponsored by
Universidade Federal Fluminense
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Dental Caries Extending Into Dentin focused on measuring Dental caries, Dentin, Pulp exposure prevention, Deep caries lesion, Conservative Treatment

Eligibility Criteria

4 Years - 6 Years (Child)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  1. The child need to be healthy;
  2. This should be in the age range of 4 to 6 years of age;
  3. The primary molars to be submitted to treatment should have the following characteristics: deep caries lesion (greater than or equal to 2/3 of dentine thickness) without clinical or radiographic aspects of pulp lesion, restoration margins above gingival line, absence of spontaneous pain or mobility, absence of periodontal changes, roots compatible with pulpal maturation stage.

Exclusion Criteria:

  1. Children under use of controlled drugs or antibiotics.
  2. Children who presented with some neurological or motor disorder that could influence the treatment procedure.
  3. Molars with more than three lost walls or margins in subgingival area.
  4. Patients with allergies to the medications used.
  5. Patients in the pulpal regression stage in which the tooth is likely to be lost within 12 months.

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm 3

    Arm Type

    Active Comparator

    Experimental

    Experimental

    Arm Label

    Indirect Pulp Capping

    Stepwise excavation

    Selective caries removal

    Arm Description

    Nonselective removal to hard dentine (formerly complete excavation or complete caries removal) : removal of soft dentin, only hard dentine is left on the cavity, so that demineralized dentine "free" of bacteria is completely removed. Intervention: Total soft and leathery caries removal. Carious dentin removal

    Stepwise removal is carious tissue removal in 2 stages, i.e., visits. Soft carious tissue is left over the pulp in the first step, while peripheral dentine is prepared to hard dentine to allow a complete and durable seal of the lesion. A provisional restoration is placed, which should be sufficiently durable to last up to 6 months to allow changes in the dentine and pulp to take place. After this period, a second excavation is done and, if there is hard dentin formed, the tooth is restored. Intervention: Part of the soft caries is removed. Final restoration is placed on the second visit. Carious dentin removal

    Selective caries removal: only part the soft dentine is removed, so soft carious tissue is left over the pulp, while peripheral enamel and dentine are prepared to hard dentine, to allow a tight seal and placement of a durable restoration. Intervention: Part of the soft caries is removed. Final restoration is place over the soft dentin. Carious dentin removal

    Outcomes

    Primary Outcome Measures

    Pulp vitality maintenance diagnosed by clinical exam
    Among the three treatment protocols, which one will have better prognosis in maintaining pulp vitality. The clinical parameters of pulpal failures are: pain, presence of abscess, fistulae and/or abnormal tooth mobility.
    Pulp vitality maintenance diagnosed by radiograph exam
    The prognosis of maintaining pulp vitality will be acessed by radiological signs of loss of vitality, as presence of abnormal root resorption and/or bone resorption.

    Secondary Outcome Measures

    Full Information

    First Posted
    August 21, 2018
    Last Updated
    August 24, 2018
    Sponsor
    Universidade Federal Fluminense
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    1. Study Identification

    Unique Protocol Identification Number
    NCT03650647
    Brief Title
    Comparison of Conventional Versus Conservative Caries Removal in Primary Teeth
    Acronym
    Caries_removal
    Official Title
    Randomized Clinical Trial Comparison of Conventional Versus Conservative Caries Removal in Primary Teeth: a Two-year Evaluation
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    August 2018
    Overall Recruitment Status
    Unknown status
    Study Start Date
    January 15, 2017 (Actual)
    Primary Completion Date
    January 15, 2018 (Actual)
    Study Completion Date
    January 5, 2020 (Anticipated)

    3. Sponsor/Collaborators

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

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Data Monitoring Committee
    Yes

    5. Study Description

    Brief Summary
    The sample will be, at least, 90 primary molars, randomly distributed into three groups: Group 1: IPC; Group 2: SE; Group 3: SCR. Teeth must present deep caries lesions (at least 2/3 of dentin depth), pulp vitality (no clinical or radiographical signs of pulp disease, such as abcesses, fistulae, root resorption, abnormal tooth mobility). This study received approval by the Ethics Committee of Fluminense Federal University (UFF; Brazil) - # CAAE: 58812816.8.0000.5626. The study started in January, 2017; and will finish in December, 2020. Patients will be selected from the public schools in Nova Friburgo. The dental exams and treatment procedures will be done at the clinics from the School of Dentistry, Health Institute of Nova Friburgo (ISNF). Laboratory proceedings will be done at: Clinical and Microbiological Research Laboratory (LAB PECMA - ISNF) - Sample storage, bacterial cultivation and identification. University of North Carolina at Chapel Hill Rio de Janeiro Federal University
    Detailed Description
    The aims of this Randomized Clinical Trial are: to evaluate the risk of pulpal exposure and tooth vitality maintenance of primary molars with deep caries lesions, treated with conservative techniques, such as Stepwise Excavation (SE) or Selective Caries Removal (SCR), and to compare with those teeth treated with Indirect Pulp Capping (IPC); to verify changes in the cultivable microbiota isolated in the deep carious dentin lesions of deciduous molars, before and after performing the procedures of SE; to clinically evaluate dentin reactions to the SE; to provide longitudinal monitoring of changes in the non-cultivable microbiota (microbiome), found in dentin carious lesions of deciduous and permanent molars, compared to the treatments performed; to determine, in vitro, the microbial metabolome of different strains isolated from dentin samples under conditions of high and low cariogenic challenge; to correlate, in vitro, the microbial metabolites with the clinical classification of the cavitated lesions from which these samples originated. The sample will be, at least, 90 primary molars, randomly distributed into three groups: Group 1: IPC; Group 2: SE; Group 3: SCR. Teeth must present deep caries lesions (at least 2/3 of dentin depth), pulp vitality (no clinical or radiographical signs of pulp disease, such as abcesses, fistulae, root resorption, abnormal tooth mobility). This study received approval by the Ethics Committee of UFF (Brazil) - # CAAE: 58812816.8.0000.5626. The study started in January, 2017; and will finish in December, 2020. Patients will be selected from the public schools in Nova Friburgo. The dental exams and treatment procedures will be done at the clinics from the School of Dentistry, Health Institute of Nova Friburgo (ISNF). Laboratory proceedings will be done at: LAB PECMA - ISNF - Sample storage, bacterial cultivation and identification University of North Carolina at Chapel Hill Rio de Janeiro Federal University

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Dental Caries Extending Into Dentin
    Keywords
    Dental caries, Dentin, Pulp exposure prevention, Deep caries lesion, Conservative Treatment

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Factorial Assignment
    Model Description
    Tooth receive one of the two test treatments: Stepwise Excavation (conservative treatment 1), Selective caries removal (conservative treatment 2) and are evaluated in parallel against a control group (indirect pulp capping treatment).
    Masking
    ParticipantInvestigatorOutcomes Assessor
    Allocation
    Randomized
    Enrollment
    49 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    Indirect Pulp Capping
    Arm Type
    Active Comparator
    Arm Description
    Nonselective removal to hard dentine (formerly complete excavation or complete caries removal) : removal of soft dentin, only hard dentine is left on the cavity, so that demineralized dentine "free" of bacteria is completely removed. Intervention: Total soft and leathery caries removal. Carious dentin removal
    Arm Title
    Stepwise excavation
    Arm Type
    Experimental
    Arm Description
    Stepwise removal is carious tissue removal in 2 stages, i.e., visits. Soft carious tissue is left over the pulp in the first step, while peripheral dentine is prepared to hard dentine to allow a complete and durable seal of the lesion. A provisional restoration is placed, which should be sufficiently durable to last up to 6 months to allow changes in the dentine and pulp to take place. After this period, a second excavation is done and, if there is hard dentin formed, the tooth is restored. Intervention: Part of the soft caries is removed. Final restoration is placed on the second visit. Carious dentin removal
    Arm Title
    Selective caries removal
    Arm Type
    Experimental
    Arm Description
    Selective caries removal: only part the soft dentine is removed, so soft carious tissue is left over the pulp, while peripheral enamel and dentine are prepared to hard dentine, to allow a tight seal and placement of a durable restoration. Intervention: Part of the soft caries is removed. Final restoration is place over the soft dentin. Carious dentin removal
    Intervention Type
    Procedure
    Intervention Name(s)
    Carious dentin removal
    Other Intervention Name(s)
    Indirect Pulp Capping, Stepwise excavation, Selective caries removal
    Intervention Description
    Carious tissue removal and managing deep cavitated carious lesions in primary teeth.
    Primary Outcome Measure Information:
    Title
    Pulp vitality maintenance diagnosed by clinical exam
    Description
    Among the three treatment protocols, which one will have better prognosis in maintaining pulp vitality. The clinical parameters of pulpal failures are: pain, presence of abscess, fistulae and/or abnormal tooth mobility.
    Time Frame
    Through study completion, up to three years.
    Title
    Pulp vitality maintenance diagnosed by radiograph exam
    Description
    The prognosis of maintaining pulp vitality will be acessed by radiological signs of loss of vitality, as presence of abnormal root resorption and/or bone resorption.
    Time Frame
    Through study completion, up to three years.

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    4 Years
    Maximum Age & Unit of Time
    6 Years
    Accepts Healthy Volunteers
    Accepts Healthy Volunteers
    Eligibility Criteria
    Inclusion Criteria: The child need to be healthy; This should be in the age range of 4 to 6 years of age; The primary molars to be submitted to treatment should have the following characteristics: deep caries lesion (greater than or equal to 2/3 of dentine thickness) without clinical or radiographic aspects of pulp lesion, restoration margins above gingival line, absence of spontaneous pain or mobility, absence of periodontal changes, roots compatible with pulpal maturation stage. Exclusion Criteria: Children under use of controlled drugs or antibiotics. Children who presented with some neurological or motor disorder that could influence the treatment procedure. Molars with more than three lost walls or margins in subgingival area. Patients with allergies to the medications used. Patients in the pulpal regression stage in which the tooth is likely to be lost within 12 months.
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Apoena A Ribeiro, PhD
    Organizational Affiliation
    University of North Carolina, Chapel Hill
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Learn more about this trial

    Comparison of Conventional Versus Conservative Caries Removal in Primary Teeth

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