Comparison of clinical and radiographic success rate of pulpotomy in primary molars using Biodentine, Endo repair and Formocresol: A double blind randomized clinical trial
Not Applicable
Recruiting
- Conditions
- Pulpitis.
- Registration Number
- IRCT20180521039763N2
- Lead Sponsor
- Kerman University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 105
Inclusion Criteria
Pulp exposure due to caries
No pathologic mobility
No history of spontaneous pain
No sinus tracts, abscess or swelling
Restorable teeth with ssc
Hemostasis could be easily achievable
No internal or pathologic external root resorption
No interradicular or periapical radiolucency
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Mutation and cytogenetic formocresol. Timepoint: 0 , 6 and 12 months later. Method of measurement: Through clinical and radiographic evaluation and questionnaire.
- Secondary Outcome Measures
Name Time Method