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

Sponsor
Armed Forces Institute of Dentistry, Pakistan
Study ID
NCT07388368
Status
Recruiting
Apply to this trial

Conditions

  • Pain

Eligibility Criteria

Sex
ALL
Age
18 Years - 60 Years
Healthy Volunteers
Not accepted

Interventions

  • Tricalcium silicate sealar — DRUG
    Ceraseal (bioceramic sealer) - assigned to Group 2
  • Resin based sealer — DRUG
    Endoplus (resin-based sealer) - assigned to Group 1

Study Details

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.

Key Dates

First listed
Feb 5, 2026
Start date
Jul 1, 2026
Status verified
Jul 2026
Primary completion
Dec 31, 2026
Completion
Jan 30, 2027

Study Design

Enrollment
118 participants (estimated)
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT

Arms

  • Active Comparator: Tricalcium silicate based sealer (Bio ceramic)
    CeraSeal bioceramic sealer will be used for obturation with matched bioceramic cones and a heated plugger (System B).
  • Experimental: Resin based sealer
    Endoplus resin-based sealer will be used for obturation with single-cone gutta-percha and a heated plugger (System B)

Primary Outcome Measure

Postoperative pain after root canal treatment assessed using a Visual Analogue Scale (VAS) [ Time Frame: 24 hours, 72 hours and 7 days ]

Central Contacts

Related Studies