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Clinical Trials/NCT05289791
NCT05289791
Completed
Not Applicable

The Effect of Ultrasonic Activation of Bioceramic Sealer on Postoperative Pain in Teeth With Symptomatic Irreversible Pulpitis: A Randomized Clinical Trial

Cairo University1 site in 1 country32 target enrollmentApril 8, 2022

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Symptomatic Irreversible Pulpitis
Sponsor
Cairo University
Enrollment
32
Locations
1
Primary Endpoint
postoperative pain
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

The aim of this study is to clinically compare post-operative pain levels after ultrasonic activation of Ceraseal bioceramic sealer versus non-activated bioceramic sealer for patients with symptomatic irreversible pulpitis related to mandibular premolar teeth.

Detailed Description

To clinically compare post-operative pain levels after ultrasonic activation of Ceraseal bioceramic sealer versus non-activated bioceramic sealer for patients with symptomatic irreversible pulpitis related to mandibular premolar teeth.Ultrasonic activation of Ceraseal bioceramic sealer for 20 seconds using non cutting ultrasonic tip.

Registry
clinicaltrials.gov
Start Date
April 8, 2022
End Date
May 2, 2023
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Bassant Yasser Shaker Ibrahim El-Saharty

principal investigator

Cairo University

Eligibility Criteria

Inclusion Criteria

  • Patients above 18 years old and to
  • Male or female.
  • Patients seeking root canal treatment.
  • Mandibular posterior teeth with Symptomatic irreversible pulpitis with preoperative sharp, moderate, or severe pain with normal periapical radiographic appearance or slight widening in lamina dura.
  • Systematically healthy patient (ASA I, II).
  • Patient who can understand modified VAS and sign informed consent

Exclusion Criteria

  • Medically compromised patients having significant systemic disorders. (ASA III or IV).
  • History of intolerance to NSAIDS.
  • Patients with two or more adjacent teeth requiring endodontic treatment.
  • External root resorption.
  • Internal root resorption.
  • Vertical root fracture.
  • Periapical lesion.
  • Association with swelling.
  • Acute peri-apical abscess or acute exacerbation of a chronic abscess.
  • Pregnancy.

Outcomes

Primary Outcomes

postoperative pain

Time Frame: 48 hours

intensity of pain on modified Visual analogue scale

Secondary Outcomes

  • Sealer Extrusion laterally and periapically(Immediately after obturation.)
  • number of analgesic tablets taken by patient after endodontic treatment(up to 48 hours postoperatively)

Study Sites (1)

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