This prospective clinical study aims to evaluate the association between the levels of selected pulpal biomarkers and the clinical success of vital pulp therapy in permanent teeth. Patients undergoing vital pulp therapy will be monitored over time, and biomarker expression levels will be analyzed in relation to treatment outcomes. The study intends to provide insight into the predictive value of pulp tissue biomarkers for long-term success in vital pulp procedures.
Who can participate
Age range16 Years – 40 Years
SexALL
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Inclusion Criteria:
* Permanent teeth diagnosed with reversible pulpitis
* Patients diagnosed with irreversible pulpitis but without apical radiolucency
* Teeth showing a normal response to cold testing (carbon dioxide snow)
* Teeth with irreversible pulpitis demonstrating prolonged response to cold testing
* Teeth with no sensitivity to percussion or chewing
* In teeth with exposed pulp tissue, bleeding time less than 5 minutes
* In irreversible pulpitis cases, bleeding time less than 10 minutes
* No widening of the periodontal ligament space (periapical index \[PAI\] ≤ 2)
* Radiographic evidence of deep dentinal caries
Exclusion Criteria:
* Teeth with a negative response to cold testing (carbon dioxide snow)
* Presence of apical radiolucency (PAI \> 2)
* Condensed apical periodontitis
* Internal or external root resorption
* History of dental trauma
* Longitudinal root fracture
* Presence of periodontal-endodontic lesions on the day of treatment
* Functional loss (e.g., Grade 3 tooth mobility)
* Swelling associated with the treated tooth
* Teeth that cannot be treated under rubber dam isolation
* Teeth from which less than 2.5 mL of pulpal blood can be collected
* Immunocompromised individuals
* Pregnant women at the time of treatment
* Use of antibiotics, bisphosphonates, or statins within 4 weeks prior to treatment
What they're measuring
1
Clinical success of treated teeth with Vital Pulp Therapy