Clinical Trials Directory

Trials / Completed

CompletedNCT07355816

Effect of Different Root Canal Disinfection Procedures on Postoperative Pain

Effect of Different Root Canal Disinfection Procedures on Postoperative Pain: A One-Week Follow-Up Clinical Study

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
80 (actual)
Sponsor
Cumhuriyet University · Academic / Other
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Not accepted

Summary

This clinical study evaluated the effects of different root canal disinfection procedures on postoperative pain. Patients requiring root canal treatment received one of several disinfection methods. Postoperative pain was assessed at 6,24, 48, 72 hours and on the 7th day using a standard pain scale. The aim of the study was to identify which method resulted in the least discomfort. Participation involved a single treatment session and short-term follow-up for pain measurement.

Conditions

Interventions

TypeNameDescription
PROCEDUREConventional Needle IrrigationRoot canals will be irrigated using a conventional syringe and needle technique with standard irrigant solutions. This method relies solely on manual delivery without activation devices.
PROCEDUREPassive Ultrasonic IrrigationRoot canals will be irrigated using passive ultrasonic activation, which uses ultrasonic energy to improve irrigant effectiveness and reduce microbial load beyond manual techniques.
PROCEDURESonic IrrigationRoot canals will be irrigated using a sonic activation device (e.g., EndoActivator) to enhance irrigant penetration and bacterial elimination compared to conventional irrigation.
PROCEDUREKTP Laser DisinfectionRoot canals will be disinfected using a KTP laser following standard irrigation protocols. Laser application aims to provide enhanced antimicrobial effects not achievable with conventional or activated irrigation methods.

Timeline

Start date
2023-06-13
Primary completion
2024-11-11
Completion
2024-11-11
First posted
2026-01-21
Last updated
2026-01-21

Locations

1 site across 1 country: Turkey (Türkiye)

Source: ClinicalTrials.gov record NCT07355816. Inclusion in this directory is not an endorsement.