This project addresses a central question within the practice of dentistry: Is a pulpotomy procedure effective in the treatment of a tooth with symptomatic irreversible pulpitis and normal periapex? In addition, the project seeks to identify clinical and molecular biomarkers that are predictive of the success of pulpotomy.
In this study, patients will be randomized to two groups. All patients will have a diagnosis of irreversible pulpitis with normal apical tissues. The groups will be root canal treatment and pulpotomy. The patients will be followed clinically and radiographically for 2 years following the treatment. Predictors of the outcome of pulpotomy will be clinical and laboratory-based parameters.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
138
School of Dentistry, University of Alabama at Birmingham
Birmingham, Alabama, United States
Percentage of patients with a successful outcome of pulpotomy versus RCT
A composite of clinical and radiographic findings and incidence of follow up procedures
Time frame: From baseline through 2 years
Determine prognostic validity of preoperative hyperalgesia in determining the outcome of pulpotomy
Neurosensory measurements of preoperative signs and symptoms will be measured and correlated with the outcome of pulpotomy
Time frame: From baseline to two years
Determine prognostic validity of a set of pulpal inflammatory proteins in determining the outcome of pulpotomy
Protein analysis at the time of treatment will be correlated with the outcome of pulpotomy
Time frame: From baseline to 2 years
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