Postoperative Pain Following Root Canal Treatment With Bioceramic Sealers
Postoperative Pain and Sealer Extrusion Following Root Canal Treatment With Neosealer Flo and Ceraseal Bioceramic Sealers; a Randomized Clinical Trial
1 other identifier
interventional
30
0 countries
N/A
Brief Summary
To evaluate and compare postoperative pain and extrusion of sealers following root canal treatment using NeoSealer Flo and CeraSeal bioceramic sealers
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started May 2026
Shorter than P25 for not_applicable
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
April 26, 2026
CompletedStudy Start
First participant enrolled
May 1, 2026
CompletedFirst Posted
Study publicly available on registry
May 8, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
September 1, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
September 8, 2026
May 8, 2026
May 1, 2026
4 months
April 26, 2026
May 3, 2026
Conditions
Keywords
Outcome Measures
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.
24 and 48 hours
Secondary Outcomes (1)
sealer extrusion
immediate postoperatively
Study Arms (2)
nanosealer flo
EXPERIMENTALbioceramic sealer
ceraseal
ACTIVE COMPARATORbioceramic sealer
Interventions
Eligibility Criteria
You may qualify if:
- Molar teeth requiring root canal treatment
- Diagnosed with symptomatic irreversible pulpitis,
- Patients able to understand and use the VAS scale
You may not qualify if:
- Patients with systemic diseases affecting pain perception
- Use of analgesics within 12 hours before treatment
- Previously treated teeth
- Teeth with periapical abscess or swelling
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Cairo Universitylead
Related Links
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- DOUBLE
- Who Masked
- PARTICIPANT, OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- clinical ass. professor, principal investigator, endodontic department
Study Record Dates
First Submitted
April 26, 2026
First Posted
May 8, 2026
Study Start
May 1, 2026
Primary Completion (Estimated)
September 1, 2026
Study Completion (Estimated)
September 8, 2026
Last Updated
May 8, 2026
Record last verified: 2026-05