Effect of concentration of irrigants on endodontic postoperative pai
Not Applicable
- Conditions
- Irreversible Pulpitis.Pulpitis
- Registration Number
- IRCT201601202016N6
- Lead Sponsor
- Vice Chancellor for Research and Technology
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 100
Inclusion Criteria
no systemic disease; first and second mandibular molar with irreversible pulpitis; normal preapical radiography; mild sensitivity to percussion; no or mild pretreatment pain; having no medication at least 6 hours before the treatment visit; age at least 18 years old; no allergic reaction to the lidocaine with epinephrine 1:80000, gelofen, and sodium hypochlorite.
Exclusion criteria: pregnancy and lactation; severe periodontal diseases; over instrumentation or overfilling; teeth that cannot be isolated; root canal calcification; root resorption; and the teeth that cannot be restored.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Postoperative pain. Timepoint: Six, 12, 24, 48, 72 hours and 4, 5, 6, 7 days following the treatment. Method of measurement: Visual analogue scale.
- Secondary Outcome Measures
Name Time Method Analgesic consumption. Timepoint: 6, 12, 24, 48, 72 hours and 4, 5, 6, 7 days following the treatment. Method of measurement: Using a specific form.