Post obturation pain seen with the use of two different sealer in a single visit root canal treatmentT

The effect of Bioactive Glass-Based and Epoxy Amine Resin Based root canal sealers on post-obturation pain in single-visit root canal treatment: A double blinded randomized controlled trial

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2023/03/050501

Enrollment

Registered

2023-03-09

Start date

Unknown

Completion date

Unknown

Last updated

2024-04-01

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

Conditions

None listed

Interventions

Intervention1: Nishika Canal Sealer BG: They generally contain alumina, zirconia particles, bioactive glass, calcium silicates, hydroxyapatite, and resorbable calcium phosphates. These ingredients all

Eligibility

Inclusion criteria

Inclusion criteria: Good oral hygiene. Patients had not used any analgesic in last 7 days. Patients had not used any antibiotic in last 7 days. Prolonged positive response to cold test (EndoIce; Coltene / Whaledent Inc, Cuyahoga Falls, OH) and electric pulp tester (Parkell, NY, USA). Patients diagnosed with asymptomatic irreversible pulpitis caused by deep carious lesion without apical periodontitis on the mandibular first or second molar teeth. The presence of profusely pulp bleeding with a thick consistency, which is exposed during caries removal. Patients who had healthy periapical tissues (confirmed with periapical radiography).

Exclusion criteria

Exclusion criteria: Patients who refused to participate in this study. Medically compromised patients (with immunosuppressive / systemic diseases, patients on medications). Symptomatic or non-vital teeth. The presence of advanced periodontal disease (probing depth > 4 mm). The presence of open apex, presence of calcification, presence of resorption. Patients who had multiple teeth requiring endodontic treatment. Patients with allergic sensitivity to materials and agents that should be used during the root canal treatment. Patients who had allergic sensitivity to local anaesthetics Patients who had systemic or allergic sensitivity for the NSAIDs. Pregnant patients and patients in lactation period. Overfilling (extrusion of the gutta-percha or sealer beyond the radiographic apex) or short filing ( > 2 mm short from the radiographic apex). The teeth with extensive coronal destruction that need a core build-up.

Design outcomes

Primary

Measure	Time frame
1. Post Operative PainTimepoint: Post operative pain will be assessed at the following time intervals during the course of the study: i.6 hours after obturation ii.24 hours after obturation iii.48 hours after obturation iv.5 days after obturation v.7 days after obturation	—

Secondary

Measure	Time frame
noneTimepoint: none	—

Countries

India

Contacts

Public ContactDr Sonali Taneja

ITS Center for Dental Studies and Research

sonalitaneja@its.edu.in9891688100

Outcome results