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Clinical Assessment of Deep Carious Lesions after Partial Removal of Caries vs Stepwise Excavation: A Randomized Controlled Trial

Not Applicable
Conditions
Oral Health
Registration Number
PACTR201603001396248
Lead Sponsor
Faculty of Oral and Dental Medicine - Cairo University
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Other
Sex
All
Target Recruitment
132
Inclusion Criteria

Patient-related criteria:
¿Patients consulting in one of the outpatient dental clinic complex, Misr International University.
¿Able to tolerate necessary restorative procedures.
¿Provide informed consent.
¿Accepts one year follow-up period.
Tooth related criteria:
¿Teeth with primary deep carious lesions involving 2/3 of the entire dentin thickness with no continuity between the carious cavity and the pulp chamber.
¿Teeth are vital according to pulp-sensitivity tests.

Exclusion Criteria

Patient-related criteria:
¿Medically compromised patients, as they will not be able to attend multiple appointments or may require special management.
¿Pregnant women; as radiographs cannot be taken for them.
¿Allergy to any of the restorative materials, including anesthetics.
¿Uncooperative patients, will not abide by the instructions or attend the appointments.

Tooth related criteria:
¿Deciduous teeth; as the study is targeting only permanent teeth.
¿Teeth with previous restorations, which may add another variable to the study (type of old restorative material, extent of recurrent caries).
¿Spontaneous pain or prolonged pain after sensitivity tests (cold and electrical tests), which would indicate irreversible pulpal damage.
¿Negative sensitivity tests, periapical radiolucencies and sensitivity to axial or lateral percussion, which would indicate pulp necrosis.
¿Teeth presenting external or internal resorption, with adverse pulpal reactions which may affect the outcome of the study.
¿Teeth with cervical caries; which can¿t be evaluated on periapical radiographs.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Maintaining pulp vitality
Secondary Outcome Measures
NameTimeMethod
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