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Active Not Recruiting NCT07834424

Direct Pulp Capping With Biodentine in Permanent Teeth With Reversible Pulpitis

Conditions: Reversible Pulpitis, Dental Pulp Exposure

Sex: All
Ages: 18 Years – N/A
Healthy volunteers: No
Phase: NA
Enrollment: 12
Sponsor: University of Medicine and Pharmacy at Ho Chi Minh City

Location: Faculty of Odonto-Stomatology, University of Medicine and Pharmacy at Ho Chi Minh City Ho Chi Minh City

Summary

This study evaluates the clinical and radiographic outcomes of direct pulp capping using Biodentine (Septodont, Saint-Maur-des-Fossés, France), a calcium silicate-based cement, in mature permanent teeth diagnosed with reversible pulpitis following carious or mechanical pulp exposure. Biodentine was placed as a full-thickness (bulk) capping and interim restoration, with a definitive composite restoration completed at a later visit. Pulp vitality, postoperative pain, and radiographic healing are assessed over a 6-month follow-up period.

Eligibility Criteria

Inclusion Criteria: * Mature permanent teeth clinically diagnosed with reversible pulpitis * Vital pulp exposure (carious or mechanical) confirmed intra-operatively * Positive response to pulp sensibility testing (cold and/or electric pulp test) at baseline * Successful haemostasis of the exposed pulp achieved within 6 minutes * Patient consent to follow-up Exclusion Criteria: * Irreversible pulpitis or pulp necrosis * Spontaneous or lingering pain * Radiographic periapical pathology * Haemostasis not achieved within the time limit * Non-restorable teeth * Teeth with periodontal compromise

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View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT07834424). StuddyBuddy aggregates publicly available trial information.