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Effect of root canal sealer on pain following root canal treatment

Effect of Resin-based and Bioceramic Root Canal Sealers on Postoperative Pain following Continuous Chelation- A Randomized Controlled Clinical Trial

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/09/045690
Enrollment
24
Registered
2022-09-20
Start date
Unknown
Completion date
Unknown
Last updated
2022-10-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: K040- Pulpitis

Interventions

Intervention1: bio ceramic sealer: placed once and evaluated at 6hrs, 12hrs, 24hrs 48hrs, 3 days, 5 days and 7 days Control Intervention1: AH sealer: placed once and evaluated at 6hrs, 12hrs, 24hrs 48

Sponsors

SRM DENTAL COLLEGE
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Good oral hygiene. 2. Patients belonging to ASA (American Society of Anesthesiologists) Category I and II. 3.Patients had not used any analgesic in last 7 days. 4. Patients had not used any antibiotic in last 7 days. 5. Patients diagnosed with symptomatic or asymptomatic irreversible pulpitis caused by deep carious lesion in the mandibular first or second molar teeth. 6. The presence of profusely pulp bleeding with a thick consistency, which is exposed during caries removing. 7. Patients who had healthy periapical tissues (confirmed with periapical radiography)

Exclusion criteria

Exclusion criteria: 1. Patients who refuse to participate in this study. 2. Medically compromised patients (with immunosuppressive / systemic diseases, patients on medications). 3.Non-vital teeth. 4. The presence of advanced periodontal disease (probing depth > 4 mm). 5. The presence of open apex, presence of calcification, presence of resorption, root caries. 6. Patients who had multiple teeth requiring endodontic treatment. 7. Patients with allergic sensitivity to materials and agents that should be used during the root canal treatment. 8. Patients who had allergic sensitivity to local anesthetics. 9. Patients who had systemic or allergic sensitivty for the NSAIDs. 10. Pregnant patients and patients in lactation period. 11. Overfilling (extrusion of the gutta-percha or sealer beyond the radiographic apex) or short filing ( > 2 mm short from the radiographic apex). 12. The teeth with extensive coronal destruction that need a core build-up. 13. Retreatment cases.

Design outcomes

Primary

MeasureTime frame
Reduction of pain when bioceramic sealer is usedTimepoint: 6, 12, 24 and 48 hours, and 3, 5, and 7 days.

Secondary

MeasureTime frame
Intake of analgesic when bioceramic sealer is usedTimepoint: 6, 12, 24 and 48 hours, and 3, 5, and 7 days.

Countries

India

Contacts

Public ContactDr S Mahalaxmi

SRM Institute of Science and Technology

researchmaha@gmail.com9381018598

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026