Viewing Study NCT05729893



Ignite Creation Date: 2024-05-06 @ 6:37 PM
Last Modification Date: 2024-10-26 @ 2:51 PM
Study NCT ID: NCT05729893
Status: RECRUITING
Last Update Posted: 2023-02-15
First Post: 2023-01-05

Brief Title: Evaluation of Post Operative Pain After Using Two Different Types of Sealers
Sponsor: British University In Egypt
Organization: British University In Egypt

Study Overview

Official Title: Evaluation of Post Operative Pain After Using Two Different Types of Sealers a Randomized Clinical Trial
Status: RECRUITING
Status Verified Date: 2023-02
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: conventional endodontic treatment is done using two different types of sealers in the obturation to evaluate the post operative pain between the two sealers
Detailed Description: STUDY WILL BE PERFORMED ON PATIENTS DIAGNOSED WITH SYMPTOMATIC IRREVERSABE PULPITIS

TREATMENT PROTOCOL FOR ALL PATIENTS IS CONVENTIONAL ROOT CANAL TREATMENT

ACCESS CAVITY AND CLEANING AND SHAPING PROCEDURES WILL BE EXECUTED FOR ALL PATIENTS WITH THE SAME PROTOCOL

SELECTED PATIENTS WILL THEN BE DIVIDED INTO TWO GROUPS

GROUP1 ALL CANALS WILL BE OBTURATED USING RESIN STANDARD SEALERS

GROUP2 ALL CANALS WILL BE OBTURATED USING HIGH FLOW BIOCERAMIC SEALERS THAT ACCEPT WARM VERTICAL COMPACTION

POST OPERATIVE PAIN IN THE TWO GROUPS WILL BE EVALUATED USING THE VISUAL ANALOUG SCALE AND COMPARED AT DIFFERENT TIME PERIODS 12H 24H 48H 72H

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