Pulp Disease, Dental
Conditions
Keywords
Direct pulp capping, Partial Pulpotomy, and Pulpotomy
Brief summary
The aim of the present study is to evaluate Mineral Trioxide Aggregate and Biodentine in direct pulp capping, partial pulpotomy, and pulpotomy in primary molars.
Detailed description
Screening of patients will continue until the target population is achieved. Identifying and recruiting potential subjects is achieved through patient database in Pediatric Dentistry department. A total of 150 primary molars from healthy subjects will be selected from the Pediatric Dentistry and Dental Public Health outpatient clinic, Faculty of Dentistry, Ain shams University. Subjects will be assigned randomly into two different treatment groups as follows: MTA Group (1): 1. Group 1(A): MTA Direct Pulp Capping. (n=25) 2. Group 1 (B): MTA Partial Pulpotomy. (n=25) 3. Group 1 (C): MTA Complete Pulpotomy. (n=25) BiodentineTM Group (2): 1. Group 2(A): BiodentineTM Direct Pulp Capping. (n=25) 2. Group 2 (B): BiodentineTM Partial Pulpotomy. (n=25) 3. Group 2 (C): BiodentineTM Complete Pulpotomy. (n=25)
Interventions
PROCEDUREDirect Pulp Capping
Direct Pulp Capping
PROCEDUREPartial Pulpotomy
Partial Pulpotomy
PROCEDUREPulpotomy
Pulpotomy
Sponsors
Ain Shams University
British University In Egypt
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)
Eligibility
Sex/Gender
ALL
Age
4 Years to 7 Years
Healthy volunteers
Yes
Inclusion criteria
* No clinical symptoms or history implying irreversible pulpitis such as spontaneous pain, or pain persisting after stimuli removal. * Absence of periapical or interadicular radiolucencies, inflammatory root resorption, sinus tract or gingival abscess.
Exclusion criteria
* Children who are extremely uncooperative and difficult to manage. * Children suffering from any physically or mentally disability that will complicate the treatment: Special Health Care needs (SHCN). * Teeth of poor prognosis due to presence of an abscess or a sinus, mobility, advanced bone or root resorption or Non-Restorable teeth.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Is to evaluate the clinical and radiographic success rates of Mineral Trioxide Aggregate and Biodentine in direct pulp capping, partial pulpotomy, and pulpotomy in primary molars. | 18 months | Is to evaluate the clinical and radiographic success rates of Mineral Trioxide Aggregate and Biodentine in direct pulp capping, partial pulpotomy, and pulpotomy in primary molars. |
Countries
Egypt
Contacts
Primary ContactMarwa Magdy, PhD
Backup ContactNadia Metwalli, Professor
Outcome results
None listed