Comparative evaluation of post-endodontic pain following root canal therapy by two different rotary instrumentation systems
Not Applicable
- Conditions
- Irreversible pulpitis.Pulpitis
- Registration Number
- IRCT2016042227519N1
- Lead Sponsor
- ministry of research and development
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 150
Inclusion Criteria
the otherwise healthy patients were aged between 20 to 50 years old with a pulpal status of irreversible pulpitis for one tooth in the upper or lower molar region.
Exclusion criteria: previous endodontic treatment; a history of drug intake including corticosteroids; opioids and NSAIDs in the previous 12 hours; pregnancy; complicated anatomy (curves greater than 25 degrees); calcifications; internal & external resorption; open apices; periodontal disease; swelling & abscess; presence of periapical lesions; sensitivity to percussion and lack of occlusal contact.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain. Timepoint: 6 hours after treatment, 12 hours after treatment, 24 hours after treatment, 48 hours after treatment and 72 hours after treatment. Method of measurement: Visual Analogue Scale questionnaire.
- Secondary Outcome Measures
Name Time Method Swelling. Timepoint: 6 hours after treatment, 12 hours after treatment, 24 hours after treatment, 48 hours after treatment and 72 hours after treatment. Method of measurement: Clinical assessment.