Assessment of post-operative pain after the use of a new sealer for performing root canal treatment.
Phase 4
- Conditions
- Health Condition 1: K040- Pulpitis
- Registration Number
- CTRI/2021/09/036338
- Lead Sponsor
- A Buvaneshwari
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Patients with irreversible pulpitis, with/ without Apical periodontitis and/ or requiring root canal treatment .
Patients having pain < 4 VAS (mild pain)
Mandibular Molar and premolar tooth with matured apex.
Periapical lesion <=3mm
Exclusion Criteria
Patient having pain > 4 VAS (moderate to severe pain)
Curved root canals > 25 degrees
Periapical lesion >= 3mm
Periodontally compromised patients
Calcified root canals
Complex root canal anatomy
Grossly destructed tooth
Chronic peri- apical abscess with or without sinus
Medically compromised patients
Patients with long term drug use
Bruxism
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method post operative pain after the use of two endodontic sealers.Timepoint: Post-operative pain data will be recorded in VAS scale at 2,4,6,8,24,48 hours through phone call to the patient.
- Secondary Outcome Measures
Name Time Method Influence of gender, pulp vitality status, periapical status and tooth type on post operative painTimepoint: Post-operative pain data will be recorded in VAS scale at 2,4,6,8,24,48 hours through