Clinical Trials Directory

Trials / Completed

CompletedNCT05289791

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

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

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
32 (actual)
Sponsor
Cairo University · Academic / Other
Sex
All
Age
18 Years – 50 Years
Healthy volunteers
Accepted

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.

Conditions

Interventions

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

Timeline

Start date
2022-04-08
Primary completion
2023-04-12
Completion
2023-05-02
First posted
2022-03-21
Last updated
2023-11-08

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT05289791. Inclusion in this directory is not an endorsement.