The comparative evaluation of ibuprofen & gabapantin on postendodontic pain.
Phase 2
- Conditions
- Accute irreversible pulpit.Pulpitis
- Registration Number
- IRCT201205069564N1
- Lead Sponsor
- Babol University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 40
Inclusion Criteria
age more than 15 years old; pian level moderate to sever(VAS more than 40mm) and clinical diagnosis reffering ireversible accute pulpitis on inferior first molar.
Exclusion criteria: antibiotic therapy one week before the study; analgesia therapy 6 hours before intervention; history of mental desease, epilepsy; consumption of any epilepsy drug and history of systemic desease.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain. Timepoint: 1 hour pre operation, hourly till 6 hours and 12, 24 and 48 hours after operation. Method of measurement: VAS.
- Secondary Outcome Measures
Name Time Method Side effect. Timepoint: Up to 2 days post treatment. Method of measurement: Question form.;Evaluation of drug efficacy. Timepoint: Up to 2days post treatment. Method of measurement: Question form.