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Clinical Trials/NCT02912286
NCT02912286
Unknown
Not Applicable

Postoperative Pain Following Irrigation With Endodontic Needle, Sonic and Passive Ultrasonic Techniques: A Randomized Controlled Trial

Cairo University0 sites57 target enrollmentJanuary 2017
ConditionsTooth,Non-vital

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Tooth,Non-vital
Sponsor
Cairo University
Enrollment
57
Primary Endpoint
postoperative pain measured by numerical rate scale
Last Updated
9 years ago

Overview

Brief Summary

The aim of this study is to compare the postoperative pain after root canal treatment following irrigation by endodontic needle, sonic and passive ultrasonic irrigation techniques.

Detailed Description

Different irrigation delivery systems are introduced to the market aiming to improve root canals disinfection. The conventional endodontic needle is commonly used because of its ease in use and good control of needle depth and irrigant volume. However it carries a higher risk of extruding the solution periapically because of positive pressure used in solution delivery. Passive ultrasonic irrigation is a noncutting irrigation technique that is done with ultrasonically activated files with continuous or intermittent flow of irrigant. It was shown that it is effective in removing remnants of pulp tissue, dentin debris and planktonic bacteria. The vibringe (Cavex Holland BV, Haarlem, the Netherlands) is an irrigation device that combines manual delivery and sonic activation of the irrigant. The aim of this study is to compare the postoperative pain after root canal treatment following irrigation by endodontic needle, sonic and passive ultrasonic irrigation techniques.

Registry
clinicaltrials.gov
Start Date
January 2017
End Date
May 2019
Last Updated
9 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Nancy Samy

Assisstant lecturer

Cairo University

Eligibility Criteria

Inclusion Criteria

  • Males or Females
  • Age between 16-60 years old
  • Permanent Mandibular molars with:
  • Non-vital response of pulp tissue
  • Absence of spontaneous pain

Exclusion Criteria

  • Pregnant females
  • Patients having significant systemic disorder
  • Patients received analgesics, anti-inflammatory or antibiotic in the last 24 hours
  • Teeth that have:
  • Vital pulp tissues
  • Association with swelling or fistulous tract
  • Acute periapical abscess
  • Greater than grade I mobility
  • Pocket depth greater than 5mm
  • Previous endodontic treatment

Outcomes

Primary Outcomes

postoperative pain measured by numerical rate scale

Time Frame: 4 hours after treatment

Numerical rate scale (NRS) consists of a line graded from 0-10 where 0 indicates no pain and 10 indicates worst pain, patient will choose the number that describe his pain level.

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