Clinical and radiographic evaluation of the efficacy of pulpal revitalization treatment: randomized clinical trial
Not Applicable
Recruiting
- Conditions
- Dental pulp necrosis/regenerationC07.793.237.315
- Registration Number
- RBR-336mnh
- Lead Sponsor
- niversidade Ceuma
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- Not specified
Inclusion Criteria
To be eligible in this study it will be necessary for patients to have the following characteristics:
Patient who volunteers to participate in the study, in the age group of 8 to 15 years; Possess at least one tooth with open apex and pulp necrosis with or without periapical lesion; Radiographic examination showing open apex with 2 mm diameter;
Healthy patient with absence of known allergies to the medicines used in the procedure, immune or systemic disease
Exclusion Criteria
Tooth with closed apex, apical cysts and existing disease requiring long-term anti-inflammatory treatment
Study & Design
- Study Type
- Intervention
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method