Postoperative Pain Following Root Canal Treatment With Bioceramic Sealers
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-60
SponsorCairo University
About this trial
To evaluate and compare postoperative pain and extrusion of sealers following root canal treatment using NeoSealer Flo and CeraSeal bioceramic sealers
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Molar teeth requiring root canal treatment
Diagnosed with symptomatic irreversible pulpitis,
Patients able to understand and use the VAS scale
Disqualifiers
Patients with systemic diseases affecting pain perception
Use of analgesics within 12 hours before treatment
Previously treated teeth
Teeth with periapical abscess or swelling
Trial design
Design model
Parallel
Treatments tested in this trial
root canal treatment
Procedure/Surgerynanosealer flo bioceramic root canal sealer
root canal treatment
Procedure/Surgerycerseral bioceramic root canal sealer
Treatment groups
30 Participants
are divided into 2 treatment groupsGroup A: nanosealer floExperimental treatment 1 intervention
Group B: cerasealActive comparator 1 intervention
Trial outcomes
Primary outcomes
1
postoperative pain
postoperative pain will be measured using a visual analogue scale ( after being introduced and discussed with the patient) at 2 time points, pain will be categorized as no pain, moderate and severe.
Time frame
24 and 48 hoursSecondary outcomes
1
sealer extrusion
sealer extrusion will be measured radiographically using standardized digital periapical posttreatment radiographs via a blinded examiner and recorded as binary outcome: present/ absent.
Time frame
immediate postoperativelyLocations
Sponsors and contacts
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Source ClinicalTrials.gov
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