Viewing Study NCT06625853



Ignite Creation Date: 2024-10-26 @ 3:41 PM
Last Modification Date: 2024-10-26 @ 3:41 PM
Study NCT ID: NCT06625853
Status: COMPLETED
Last Update Posted: None
First Post: 2024-10-01

Brief Title: XP-Endo Finisher on Postoperative Pain in Retreatment Cases Using Mtwo R Files
Sponsor: None
Organization: None

Study Overview

Official Title: Supplementary Use of the XP-Endo Finisher on Postoperative Pain in Retreatment Cases Using Mtwo R Files Randomized Clinical Trial
Status: COMPLETED
Status Verified Date: 2024-10
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: No
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: Introduction Postoperative pain is one of the most critical issues in our daily practice postoperative pain control is essential for patient satisfaction and comfort When primary root canal treatment fails root canal retreatment aims to heal apical periodontitis

Aim of study To compare between postoperative pain POS after endodontic retreatment using NI-TI rotary files Mtwo R alone and in conjunction with XP endo finisher

Materials and Methods This research is a randomized clinical trial conducted in a parallel design on 50 patients needing retreatment They will be divided into two groups group 1 retreatment with Mtwo R group 2 retreatment with Mtwo R followed by Xp - Endo finisher Postoperative pain levels will be evaluated at 24 hours 48 hours 72 hours and 7 days following the removal of the obturation mat erial The assessment of pain will be done through clinical examination The Defense and veterans pain rating scale DVPRS and by the intake of pain killer
Detailed Description: None

Study Oversight

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