Viewing Study NCT06020911



Ignite Creation Date: 2024-05-06 @ 7:29 PM
Last Modification Date: 2024-10-26 @ 3:07 PM
Study NCT ID: NCT06020911
Status: COMPLETED
Last Update Posted: 2024-05-01
First Post: 2023-08-23

Brief Title: Indirect Pulp Capping Using Biodentine and Theracal Light-cured in Primary Molars
Sponsor: Tanta University
Organization: Tanta University

Study Overview

Official Title: Clinical and Radiographic Evaluation of Indirect Pulp Capping Using Biodentine and Theracal Light-cured in Primary Molars
Status: COMPLETED
Status Verified Date: 2024-04
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: this study is aimed to conduct tomographic evaluation of reparative dentin bridges formed after indirect pulp capping with Biodentine and Theracal light cured The null hypothesis of the study is that there will be no difference in the quantity and quality of reparative dentin formation between the tested materials used for the indirect pulp capping
Detailed Description: Many materials have been used in indirect pulp capping for primary dentition An ideal pulp capping material is to be successful when it is biocompatible radiopaque maintain good seal protect the pulp against bacterial invasion in both long and short run release sustained amounts of calcium ions act as reservoir for calcium hydroxide and stimulate reparative dentin formation through inducing the pulp cells to form odontoblasts

Theracal light cured is a light-cured resin modified calcium silicate RMCS used as an indirect pulp capping material It releases more calcium ions than Mineral trioxide aggregate or dycal inducing reparative dentin and dentin bridge formationTheracal light cured showed better sealing ability and less microleakage than Mineral trioxide aggregate and Biodentine

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None