RecruitingNot ApplicableNCT07256691

Effect of Calcium-Based Bioceramic Sealer and Resin-Based Sealer on Postoperative Pain

Effect of Calcium-Based Bioceramic Sealer and Resin-Based Sealer on Postoperative Pain in Adults With Asymptomatic Apical Periodontitis


Sponsor

Fatima Memorial Hospital

Enrollment

60 participants

Start Date

Dec 1, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

This study aims to compare the effect of calcium-based bioceramic sealer and resin-based sealer on postoperative pain in adult patients with asymptomatic apical periodontitis undergoing root canal treatment. Asymptomatic apical periodontitis is a condition where the tissue around the tip of the tooth root is inflamed or shows a lesion on X-ray, but the patient does not experience pain. A total of 60 patients will be randomly assigned to receive root canal treatment with either the bioceramic sealer (Group A) or the resin-based sealer (Group B). Pain after treatment will be measured using a 0-10 Numeric Pain Rating Scale at 4, 24, and 48 hours post-treatment. The highest pain score reported will determine whether the treatment is considered a success (no or mild/moderate pain) or failure (severe pain). The results of this study will provide evidence on which sealer is associated with less postoperative pain, helping clinicians make informed decisions about root canal filling materials.


Eligibility

Min Age: 18 YearsMax Age: 55 Years

Plain Language Summary

Simplified for easier understanding

This study compares two different materials used to seal the inside of a tooth root during a root canal — a calcium-based material versus a resin-based material — to see which one causes less pain afterward. **You may be eligible if...** - You are 18 to 55 years old - Your tooth has been diagnosed with a dead nerve (non-vital pulp) and no active pain - Your tooth has no current symptoms like pain when tapping or pressing - Your tooth root is fully formed with no signs of active infection at the tip **You may NOT be eligible if...** - You have pain or tenderness in the tooth before treatment - Your tooth has an incomplete root or active infection at the root tip - You have allergies to the materials being studied - You are pregnant or taking medications that affect pain perception Talk to your doctor to see if this trial is right for you.

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

PROCEDUREResin-based sealer obturation technique

Root canal obturation using resin based sealer with single cone GP technique. Canals prepared and irrigated as above. Pain recorded at 4, 24, and 48 hours post-obturation using NPRS.

PROCEDUREBioceramic sealer obturation

Participants in this group will undergo root canal obturation using a calcium silicate based bioceramic sealer with a single-cone gutta percha technique. After standard canal preparation and irrigation with 2.5% sodium hypochlorite, the canals will be dried with paper points. The bioceramic sealer will be applied using a lentulospiral or directly coated on the master gutta-percha cone. A matched-taper gutta-percha cone will then be inserted to full working length. The canal orifice will be sealed with a temporary or permanent restoration. Postoperative pain will be assessed at 4, 24, and 48 hours using the Numeric Pain Rating Scale (NPRS).


Locations(1)

Fatima Memorial Hospital

Lahore, Punjab Province, Pakistan

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NCT07256691


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