Comparison of Conventional Versus Conservative Caries Removal in Primary Teeth

Dental Caries Extending Into Dentin Clinical Trial

— Caries_removal  

Official title:

Randomized Clinical Trial Comparison of Conventional Versus Conservative Caries Removal in Primary Teeth: a Two-year Evaluation

Clinical Trial Details — Status: Active, not recruiting

Administrative data

• NCT number: NCT03650647
• Other study ID #: ARibeiro
• Status: Active, not recruiting
• Phase: N/A
• Start date: January 15, 2017
• Est. completion date: January 5, 2020

Study information

• Verified date: August 2018
• Source: Universidade Federal Fluminense
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial 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

Description:

The aims of this Randomized Clinical Trial are:

1. 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);

2. 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;

3. to clinically evaluate dentin reactions to the SE;

4. 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;

5. to determine, in vitro, the microbial metabolome of different strains isolated from dentin samples under conditions of high and low cariogenic challenge;

6. 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

Recruitment information / eligibility

• Status: Active, not recruiting
• Enrollment: 49
• Est. completion date: January 5, 2020
• Est. primary completion date: January 15, 2018
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 4 Years to 6 Years

Eligibility

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.

Related Conditions & MeSH terms

• Dental Caries
• Dental Caries Extending Into Dentin

Intervention

Procedure:
• Carious dentin removal
Carious tissue removal and managing deep cavitated carious lesions in primary teeth.

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
Universidade Federal Fluminense

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	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.	Through study completion, up to three years.
Primary	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.	Through study completion, up to three years.