Status:

COMPLETED

Effect of Ultrasonic Activation of Bioceramic Sealer on Postoperative Pain in Lower Premolars

Lead Sponsor:

Cairo University

Conditions:

Symptomatic Irreversible Pulpitis

Eligibility:

All Genders

18-50 years

Phase:

NA

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...

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 re...

Eligibility Criteria

Inclusion

  • Patients above 18 years old and to 50.
  • 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

  • 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.
  • Use of ibuprofen in the last 12 hour.
  • Bleeding disorder.
  • Long term corticosteroid use.
  • Mobility Grade II or III.
  • Pocket depth more than 5mm.
  • Previous root canal therapy.
  • Non-restorability.
  • TMJ problems, bruxism, clenching or traumatic occlusion.
  • Inability to perceive the given instructions

Key Trial Info

Start Date :

April 8 2022

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

May 2 2023

Estimated Enrollment :

32 Patients enrolled

Trial Details

Trial ID

NCT05289791

Start Date

April 8 2022

End Date

May 2 2023

Last Update

November 8 2023

Active Locations (1)

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1

Cairo university

Giza, Manial, Egypt