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UnknownNCT05102318

Clinical and Radiographic Evaluation of Mineral Trioxide Aggregate and Biodentine as Pulp Medicaments in Primary Molars

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
150 (estimated)
Sponsor
British University In Egypt · Academic / Other
Sex
All
Age
4 Years – 7 Years
Healthy volunteers
Accepted

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)

Conditions

Interventions

TypeNameDescription
PROCEDUREDirect Pulp CappingDirect Pulp Capping
PROCEDUREPartial PulpotomyPartial Pulpotomy
PROCEDUREPulpotomyPulpotomy

Timeline

Start date
2020-04-01
Primary completion
2022-04-01
Completion
2022-09-01
First posted
2021-11-01
Last updated
2022-02-11

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT05102318. Inclusion in this directory is not an endorsement.