The purpose of this randomized clinical trial is to compare the clinical/radiographic success of Hall technique and modified Hall technique in the treatment of primary molars with deep dentine carious lesions in children (3-12-year-old). The secondary aim is to examine the effect of marginal ridge breakdown level on treatment success.
Who can participate
Age range3 Years – 12 Years
SexALL
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Inclusion Criteria:
* Medically healthy children
* Participants attending follow-up appointments
* Children having at least one primary molar tooth with deep dentin caries involving occluso proximal surfaces.
Tooth inclusion criteria:
* Vital pulp with symptom-free or reversible pulpitis
* Presence of marginal ridge breakdown and accessible cavity with hand instruments,
* Presence of active cavitated carious lesion (Code 3 with Nyvad criteria for caries lesion activity and severity assessment- Nyvad et al., 1999)
* Absence of spontaneous or prolonged pain related with irreversible pulpitis
* Absence of fistula or abscess near the tooth
* Absence of pathological mobility
* Absence of pain on percussion
* Absence of pulp exposure
* Caries lesion located in ½ inner part of dentin radiographically
* Presence of sound dentin layer between the deepest part of the carious lesion and the pulp radiographically
* Absence of periapical or furcation pathologies on radiographs
* Absence of internal and external root resorption on radiographs
* More than ½ of root remaining
Exclusion Criteria:
* Any systemic disease, physical or mental disorder
* Children or parents who doesn't accept to participate and sign the informed consent
* Clinical or radiographic signs of pulpal or peri-radicular pathology
* Caries cavity which cannot be accessible to hand instruments
* Physiological root resorption more than 1/2 of the root in primary molars
What they're measuring
1
Clinical and radiographic success of the treatments
Timeframe: Change from baseline up to 3, 6 and 12 months