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

NCT05289791 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 32

Last updated 2023-11-08

No results posted yet for this study

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.

Conditions

  • Symptomatic Irreversible Pulpitis

Interventions

OTHER

ultrasonic activation of bioceramic sealer

activation of bioceramic sealer using ultrasonic tip for 20 seconds in buccolingual and mesiodistal direction

Sponsors & Collaborators

  • Cairo University

    lead OTHER

Principal Investigators

  • Heba M. El-far, professor · Cairo University

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

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

Timeline & Regulatory

Start
2022-04-08
Primary Completion
2023-04-12
Completion
2023-05-02

Countries

  • Egypt

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 NCT05289791 on ClinicalTrials.gov