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Partial Removal of Caries Dentines

Alternative Treatment of Deep Caries Lesions Based on Biological Evidences

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00887952
Acronym
PRCD
Enrollment
329
Registered
2009-04-24
Start date
2005-08-31
Completion date
2010-11-30
Last updated
2009-12-30

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

Conditions

Dental Caries

Keywords

Deep caries lesion, dentine caries removal, dental restoration, stepwise excavation

Brief summary

The aim of this multicenter randomized controlled clinical trial is to evaluate the effectiveness of an alternative treatment for deep caries lesions in Public Health Services. The alternative treatment consists of partial removal of carious dentine followed by restoration. The subjects were assigned to test or control groups: test - carious dentine partial removal and restoration in one session, and control - stepwise excavation. The stepwise excavation consists of partial removal of carious tissue from the cavity floor, indirect pulp capping with calcium hydroxide cement; temporary filling; cavity re-opening after 60 days, removal of the remaining soft carious tissue and filling. Each group was divided according to the filling material: amalgam or resin. The radiological exams are being performed before and after the treatment and then annually. Clinical evaluation of the restorations is performed right after the treatment and then annually (modified USPHS System). All evaluations are performed by calibrated and trained dentists.

Interventions

PROCEDUREPartial removal of carious dentine

All procedures will be carrying out under local anesthesia and rubber dam. The treatment will be performed as follow: access to the lesion using rotator instruments (if necessary); fully removal of carious tissue from the cavity walls according to hardness criteria by rotator instruments and/or hand excavator; removal of the necrotic carious tissue (soft and disorganized carious tissue) from the cavity floor by hand excavator (to avoid pulp exposure); cleaning with distilled water and drying with sterile filter paper; group randomization. If the tooth is assigned to test group: cavity floor covered with calcium hydroxide cement; restoration using amalgam or steel crown following their usual clinical procedures based on the instructions of the manufacturer

The treatment will be performed as follow: access to the lesion using rotator instruments (if necessary); fully removal of carious tissue from the cavity walls according to hardness criteria by rotator instruments and/or hand excavator; removal of the necrotic carious tissue (soft and disorganized carious tissue) from the cavity floor by hand excavator (to avoid pulp exposure); cleaning with distilled water and drying with sterile filter paper; group randomization. If the tooth is assigned to SE: indirect pulp capping with calcium hydroxide cement; temporary filling with IRM; cavity re-opening after 60 days, removal of the remaining soft carious tissue and filling following the same procedures described to test group.

Sponsors

Fundação de Amparo à Pesquisa do Estado do Rio Grande do Sul, Brazil
CollaboratorOTHER
Conselho Nacional de Desenvolvimento Científico e Tecnológico
CollaboratorOTHER_GOV
Ivoclar Vivadent AG
CollaboratorINDUSTRY
Federal University of Rio Grande do Sul
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
9 Years to 45 Years
Healthy volunteers
No

Inclusion criteria

* patients ≥ nine years old; * permanent molars with primary deep caries lesion reaching dentine inner half (radiographic exam); * pulpal sensibility positive (cold test); * absence of spontaneous pain; * absence of periapical alterations (radiographic exam); * negative percussion test.

Exclusion criteria

* subjects with general diseases affecting their caries experience; * caries lesion evolving an entire cusp; * caries lesion with cervical margin in dentine.

Design outcomes

Primary

MeasureTime frame
Pulp sensitivityOnce a year during at least five years

Secondary

MeasureTime frame
Remineralization of the residual caries (measure through digital substraction of radiographic exams)Once a year during at least five years
Cost-effectiveness analysisDuring five years of follow-up
Clinical evaluation of amalgam and resin restorations (USPHS criteria)Once a year during at least five years

Countries

Brazil

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 25, 2026