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

StatusRecruiting
PhaseNot applicable
Started
View on ClinicalTrials.gov ↗
Trial flagged as At Risk
Primary completion moved at least 4 months later Aug 1, 2026 → Dec 31, 2026
See other at-risk trials from Armed Forces Institute of Dentistry, Pakistan

Record History

  1. Notable Recruitment openedv2 Show 4 more changesShow less
    • Start date changed from estimate of Feb 1, 2026 to Jul 1, 2026
    • Primary completion pushed from Aug 1, 2026 to Dec 31, 2026
    • Study completion moved earlier from Aug 1, 2027 to Jan 30, 2027
    • Site details revised
  2. Minor Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
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.
Trial Details
NCT Number NCT07388368
Lead Sponsor Armed Forces Institute of Dentistry, Pakistan
Conditions
(from sponsor)
Pain
Related terms Pain
Enrollment 118 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov