Viewing Study NCT05928858



Ignite Creation Date: 2024-05-06 @ 7:11 PM
Last Modification Date: 2024-10-26 @ 3:02 PM
Study NCT ID: NCT05928858
Status: NOT_YET_RECRUITING
Last Update Posted: 2023-08-01
First Post: 2023-06-24

Brief Title: Clinical And Radiographic Evaluation Of Premixed Bio-ceramic MTA In Indirect Pulp Capping Of Young Permanent Molars
Sponsor: Cairo University
Organization: Cairo University

Study Overview

Official Title: Clinical And Radiographic Evaluation Of Premixed Bio-ceramic Mineral Trioxide Aggregate Versus Calcium Hydroxide In Indirect Pulp Capping Of Young Permanent Molars A Randomized Controlled Trial
Status: NOT_YET_RECRUITING
Status Verified Date: 2023-07
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: The present study aims to evaluate the clinical and radiographic success of premixed bio-ceramic MTA versus calcium hydroxide in indirect pulp capping of young permanent molars
Detailed Description: Researchers are still in search of an ideal material for pulp capping and they evaluated numerous dental materials For many decades calcium hydroxide has been the gold standard material for maintaining pulp vitality Both clinically and histologically it has been found to produce satisfactory results in indirect and direct pulp capping because it can stimulate the formation of tertiary dentine by the pulp and it has antimicrobial properties

Due to the drawbacks of calcium hydroxide several materials have been developed such as NeoPUTTY which is premixed bio-ceramic Mineral Trioxide Aggregate MTA that triggers hydroxyapatite Its firm non-tacky consistency wash-out resistance and bioactivity make it a pediatric dentists preferred material for every pulp need It also delivers ready-to-use material for immediate placement with zero waste saving cost and chair time

Study Oversight

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