Evaluation of analgesic effects of diclofenac sodium and ketorolac in root canal therapy
Phase 3
Recruiting
- Conditions
- pain in tooth.Acute apical periodontitis of pulpal originK04.4
- Registration Number
- IRCT20180513039638N1
- Lead Sponsor
- Oroumia University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 45
Inclusion Criteria
patient who requires root canal treatment of the first mandibular molars with irreversible pulpitis Between the ages of 18 and 60
Exclusion Criteria
Being in late pregnancy or breastfeeding
Having Asthma or any allergies to diclofenac sodium or ketorolac
History of gastrointestinal diseases such as stomach ulcers
History of Bleeding disorders
Intention to perform heart bypass surgery after receiving medication
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Intensity of pain. Timepoint: Measurement of patient's toothache immediately before treatment and at 6, 12 and 24 hours after treatment. Method of measurement: Visual Analog Scale Pain Assessment Form.
- Secondary Outcome Measures
Name Time Method