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Postoperative Pain After Using NiTi Instruments

NCT04700995 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 180

Last updated 2021-01-13

No results posted yet for this study

Summary

The aim of this randomized clinical trial was to compare the incidence, intensity and duration of postoperative pain following the removal of root canal obturation materials canals using rotary (ProTaper Universal or Hyflex EDM) or reciprocating file (Reciproc Blue or WaveOne Gold) systems. The null hypothesis tested was that there is no difference in postoperative pain following the retreatment procedure between the four systems used.

Conditions

  • Post-Op Complication
  • Endodontic Inflammation
  • Endodontically Treated Teeth
  • Apical Periodontitis

Interventions

PROCEDURE

NiTi instruments

Root canal filling removal

Sponsors & Collaborators

  • Trakya University

    lead OTHER

Principal Investigators

  • Burhan Çanakçi · Trakya University, Faculty of Dentistry

  • Özgür Er · Trakya University, Faculty of Dentistry

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
60 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2020-05-01
Primary Completion
2020-09-01
Completion
2020-09-10

Countries

  • Turkey (Türkiye)

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04700995 on ClinicalTrials.gov