Post obturation pain seen with the use of two different sealer in a single visit root canal treatmentT
- Registration Number
- CTRI/2023/03/050501
- Lead Sponsor
- Dr Ritesh Nagpal
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 78
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).
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.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1. Post Operative PainTimepoint: Post operative pain will be assessed at the following time intervals during the course of the study: <br/ ><br>i.6 hours after obturation <br/ ><br>ii.24 hours after obturation <br/ ><br>iii.48 hours after obturation <br/ ><br>iv.5 days after obturation <br/ ><br>v.7 days after obturation <br/ ><br>
- Secondary Outcome Measures
Name Time Method noneTimepoint: none