Clinical Trials Directory

Trials / Completed

CompletedNCT03708081

Comparative Evaluation of Different File Systems in Postoperative Pain

Comparative Evaluation of Different File Systems in Postoperative Pain: Randomize Clinical Study

Status
Completed
Phase
Study type
Observational
Enrollment
60 (actual)
Sponsor
Bulent Ecevit University · Academic / Other
Sex
All
Age
Healthy volunteers

Summary

Postoperative pain is a frequent complication associated with root canal treatment. The apical extrusion of irrigant and debris, including bacteria and necrotic tissue, may lead to postoperative pain, periapical inflammation, and flare-ups. The instrumentation technique and the file design may affect the amount of debris extrusion. The aim of this study was to evaluate the influence of instrumentation techniques on the incidence and intensity of postoperative pain after single-visit root canal treatment.

Detailed description

Sixty patients having root canal treatment indication and a single root canal were included in the study. The patients were randomly assigned into 2 groups according to root canal instrumentation technique used. In group 1; ProTaper Next (Dentsply Maillefer, Ballaigues, Switzerland) instruments with rotational motion, in group 2 TF Adaptive (SybronEndo, Orange, CA) instruments with adaptive motion were used for root canal treatments. Root canal treatment was carried out in a single visit and the severity of postoperative pain was assessed via a four-point pain intensity scale. All the participants were called through the phone at 12, 24 and 48h to obtain the pain scores. Data were analyzed using the Mann Whitney-U, Friedman and Wilcoxon tests.

Conditions

Interventions

TypeNameDescription
PROCEDUREProTaper NextRoot canal instrument
PROCEDURETF AdaptiveRoot canal instrument

Timeline

Start date
2017-06-01
Primary completion
2018-09-10
Completion
2018-10-05
First posted
2018-10-17
Last updated
2018-12-20

Locations

1 site across 1 country: Turkey (Türkiye)

Source: ClinicalTrials.gov record NCT03708081. Inclusion in this directory is not an endorsement.