← Back to Clinical Trials
Recruiting NCT07388368

NCT07388368 Comparative Evaluation of Post Obturation Pain After Root Canal Treatment Using Tricalcium Silicate vs Resin-Based Sealers

◆ AI Clinical Summary
Plain-language summary for patients
Clinical Trial Summary
NCT ID NCT07388368
Status Recruiting
Phase
Sponsor Armed Forces Institute of Dentistry, Pakistan
Condition Pain
Study Type INTERVENTIONAL
Enrollment 118 participants
Start Date 2026-07-01
Primary Completion 2026-12-31

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age 60 Years
Study Type INTERVENTIONAL
Interventions
Tricalcium silicate sealarResin based sealer

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 118 participants in total. It began in 2026-07-01 with a primary completion date of 2026-12-31.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief 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 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

Contact & Investigator

Central Contact

Pooja Kumari

✉ dhomejapooja@gmail.com

📞 03133422793

Frequently Asked Questions

Who can join the NCT07388368 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, up to 60 Years, studying Pain. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07388368 currently recruiting?

Yes, NCT07388368 is actively recruiting participants. Contact the research team at dhomejapooja@gmail.com for enrollment information.

Where is the NCT07388368 trial being conducted?

This trial is being conducted at Rawalpindi, Pakistan.

Who is sponsoring the NCT07388368 clinical trial?

NCT07388368 is sponsored by Armed Forces Institute of Dentistry, Pakistan. The trial plans to enroll 118 participants.

Related Trials

ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: September 2026  ·  Data Methodology