Effect of preemptive ibuprofen analgesic compared to placebo on pain perception associated with the placement of temporary anchorage devices (TADs), A double blinded randomised clinical trial
Phase 3
- Conditions
- Malocclusion, Dental crowding..Anomalies of dental relationship
- Registration Number
- IRCT20210803052059N1
- Lead Sponsor
- Tabriz University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 46
Inclusion Criteria
Patients treated with fixed orthodontic appliances
Patients that only need one TAD in the posterior part of the maxilla
Patients that will agree to participate in the clinical trial
Exclusion Criteria
Patients with poor oral hygiene or severe gingivitis
Patients with systemic diseases
Patients who currently are using other pain killer medications
Patients who are allergic to any of TAD, Ibuprofen, or Placebo medication
Patients who can not swallow
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Severity and type of pain during different times. Timepoint: severity and type of pain will be recorded at the following times: immediately after TAD placement (T1), 1 hour after TAD placement (T2), 12 hours after TAD placement (T3), 24 hour after TAD placement (T4). Method of measurement: The patients will be asked to fill a questionnaire form, this form is consisted of a Persian translated copy of short form of McGill Pain questionnaire (SF-MPQ).
- Secondary Outcome Measures
Name Time Method