comparison of analgesic drug and laser effect on pain reduction after orthodontic separator implementatio
Not Applicable
- Conditions
- orthodontic pain.Disorder of teeth and supporting structures, unspecified
- Registration Number
- IRCT2016061316582N2
- Lead Sponsor
- Vice Chancellor for Research and Technology, Hamedan University of Medical Science
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 60
Inclusion Criteria
Patients between13-25 years old;Female patients not to be pregnant; Patients with no orthodontic treatment history; Patients with no gelofen reaction history in the drug group; In the drug group the minimum weight should be 40 kg.
Exclusion criteria: patients with history of systemic disease; Patients with periodontal disease, More than 3 mm Probing depth; Attached gingiva recession; Using antibiotic in drug group .
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The pain after seprator placement. Timepoint: Immediately after the intervention, 6 hours after intervention, 12 hours after intervention, 24 hours after intervention,2 days after intervention,3 days or more after intervention. Method of measurement: Questionnaire Modified McGill.
- Secondary Outcome Measures
Name Time Method