RecruitingNot ApplicableNCT07388368

Comparative Evaluation of Post Obturation Pain After Root Canal Treatment Using Tricalcium Silicate vs Resin-Based Sealers

A Comparative Evaluation of Post Obturation Pain After Root Canal Treatment Using Tricalcium Silicate Versus Resin-based Sealers in Cases With Symptomatic Irreversible Pulpitis

Sponsor

Armed Forces Institute of Dentistry, Pakistan

Enrollment

118 participants

Start Date

Jul 1, 2026

Study Type

INTERVENTIONAL

Conditions

Pain

Summary

This is a randomized controlled trial comparing the mean and standard deviation of postobturation pain using two different sealers: a tricalcium silicate-based sealer (CeraSeal) and a resin-based sealer (Endoplus) in patients with symptomatic irreversible pulpitis undergoing root canal treatment.

Eligibility

Min Age: 18 YearsMax Age: 60 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a drug called Resin based sealer and a drug called Tricalcium silicate sealar for people with pain. The study is currently recruiting participants at 1 location. People eligible for this study include aged 18 Years to 60 Years.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGTricalcium silicate sealar

Ceraseal (bioceramic sealer) - assigned to Group 2

DRUGResin based sealer

Endoplus (resin-based sealer) - assigned to Group 1

Locations(1)

Armed Force Institute of Dentistry

Rawalpindi, Punjab Province, Pakistan

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NCT07388368

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