Clinical trial Recruiting at 1 site Interventional Ages 18 to 60

Post Obturation Pain After Root Canal: Bioceramic Sealer vs Resin-Based Sealer

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

Run by Armed Forces Institute of Dentistry, Pakistan · NCT07388368 · Data updated 2026-11-12

This trial tests whether a bioceramic sealer (CeraSeal) reduces pain after root canal obturation compared with a resin-based sealer (Endoplus) in adults with symptomatic irreversible pulpitis.

Quick facts

Study typeInterventional
Ages18 Years to 60 Years
SexAll
Enrollment118 (estimated)
SponsorArmed Forces Institute of Dentistry, Pakistan
Academic / other
Locations1 site (Rawalpindi, Punjab Province)
StatusRecruiting
StartedJuly 1, 2026
Main results expectedDecember 31, 2026
Study endsJanuary 30, 2027
Registry record updatedJuly 29, 2026
Trial IDNCT07388368 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults 18–60 with symptomatic irreversible pulpitis requiring root canal treatment, healthy enough for standard dental procedures (ASA I–II).

Probably not a fit

Patients with complex canal anatomy, contraindications to sealing materials, or those who do not respond to standard pain management may not benefit.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This randomized controlled trial compares two root canal sealers to see which one leads to less post-obturation pain. Adults aged 18–60 with ASA I–II and symptomatic irreversible pulpitis are eligible and will be randomly assigned to receive either Endoplus (resin-based) or CeraSeal (tricalcium silicate/bioceramic) as the sealer. Procedures are standardized and performed by the principal investigator, including anesthesia, isolation, chemo-mechanical prep, medicament placement, and obturation. The primary outcome is mean post-obturation pain with its standard deviation, measured after treatment. Ethical approval will be obtained, informed consent collected, and participants followed up to ensure safety and data integrity.

Why it matters

Potential benefit: If successful, patients may experience less pain after root canal treatment with the bioceramic sealer, improving comfort and recovery.

How similar studies have gone: Previous studies have explored different sealers, but direct head-to-head pain outcomes between bioceramic and resin-based sealers remain limited, making this approach relatively novel.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* • Patients of age group 18 to 60 years

  * Healthy patients with ASA class 1 and 2
  * Patients of both genders
  * Teeth diagnosed as symptomatic irreversible pulpitis
  * Single as well as multirooted teeth

Exclusion Criteria:

* Teeth with calcified or previously treated canals
* Immunocompromised or mentally handicapped patients
* Pregnant or lactating mothers
* Teeth with periodontal probing depths of 5 mm or more
* Cracked or un restorable teeth
* Teeth where root canal instrumentation could not reach within 2 mm of the radiographic apex

Where it's running

  • Armed Force Institute of Dentistry
    Rawalpindi, Punjab Province, Pakistan
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.