Effect of different factors on the in-operative relief pain in root canal therapy
- Conditions
- Irreversible Pulpitis.Pulpitis
- Registration Number
- IRCT201611242016N7
- 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
Age 18 or more than 18 years, no contraindications to taking either Ibuprofen (history of any allergic reaction to aspirin, NSAIDS, or Lidocaine with Epinephrine, nasal polyp, history of peptic ulcers or GI bleeding, pregnancy and lactation, renal or hepatic disease), no history of GI disorders or ulcer, having no serious systemic disease.
Exclusion criteria: no response to cold test, having sensitivity to percussion and palpation, having radiographic changes such as PDL widening, lack of vital pulp in coronal pulp chamber access cavity preparation, teeth with evidence of crack in their crown, having advanced periodontal disease, taking narcotic drugs or analgesic drugs in recent 24 hours before treatment.
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Response to cold test. Timepoint: Before taking drug, 1 hour after taking drug before anesthetic injection, after local anesthetic injecyion. Method of measurement: Cold spray.
- Secondary Outcome Measures
Name Time Method In-operative pain. Timepoint: In access cavity preparation and during treatment. Method of measurement: Using Visual Analogue Scale (VAS).