Viewing Study NCT06545773



Ignite Creation Date: 2024-10-26 @ 3:37 PM
Last Modification Date: 2024-10-26 @ 3:37 PM
Study NCT ID: NCT06545773
Status: COMPLETED
Last Update Posted: None
First Post: 2024-08-01

Brief Title: Postoperative Pain After Conservative Root Canal Preparation
Sponsor: None
Organization: None

Study Overview

Official Title: Effect of Conservative Root Canal Preparation on Postoperative Pain A Randomised 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: The goal of this clinical trial is to compare the pain experienced by healthy participants after root canal treatment with small versus large root canal sizes

The main questions it aims to answer are

1 Do small and large root canal sizes cause different pain levels
2 What is the number of painkiller pills taken by each participant
3 Does small root canal size cause severe pain and facial swelling

The researcher will perform root canal treatment on lower molar teeth The researcher will ask about the pain level painkiller pill number and swelling on the 6th12th 24th 48th 72nd hours and 7th day after the treatment
Detailed Description: Root canal shaping is an essential step for root canal treatment Necrotic tissues debris microorganisms and organic matter should be removed to clean and disinfect the root canals Previously this conventional procedure involved removing excessive dentine from root canals which weakened the tooths structural integrity Due to technological advances excessive dentine removal is not always necessary Root canals are claimed to be disinfected despite minimal dentine removal This concept of treatment is called minimally invasive or conservative root canal treatment

This study compares postoperative pain after conservative and conventional root canal preparation in healthy participants with necrotic mandibular molars

Participants will be enrolled after clinical and radiographic examination by an independent endodontist and allocated randomly to conventional or conservative root canal treatment groups After the root canal treatment the researcher will send the participants an online questionnaire on the 6th12th 24th 48th and 72nd hours and 7th day and ask them to rate their pain score according to the Numerical Rating System and the number of painkillers they have taken The flare-up rate will be determined according to the presence of swelling and severe pain

An experienced endodontist not involved in the research will monitor eligible participants and clinical treatment protocol

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