Pain reduction after using different activation systems of irrigants used in RCT
Phase 3
- Conditions
- Health Condition 1: K040- Pulpitis
- Registration Number
- CTRI/2021/09/036154
- Lead Sponsor
- Faculty of Dental Sciences IMS BH
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1.Age >18 years
2.Subject must not have taken any medication in pain in the previous 10 days prior to treatment
3.All patients reported moderate to severe pain of either continuous or spontaneous
nature, nocturnal incidence, radiating or throbbing pain.
4.All teeth included in the study responded to cold pulp sensibility tests
with an exaggerated response or pain with/without lingering
Exclusion Criteria
1.Presence of Any systemic Condition
2.Presence of any periapical bone changes on the pre-operative periapical radiographs
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To analyse reduction in VAS Pain scores.Timepoint: 24 hours, 48 hours
- Secondary Outcome Measures
Name Time Method Reduction pain and discomfortTimepoint: 24hours, 48 hours