The Comparison of the amount of pain from immediate and delayed palatal injection following buccal infiltrate injection using two anesthetic drugs
Phase 3
- Conditions
- ocal anaesthetics.Local anaesthetics
- Registration Number
- IRCT2016071817880N4
- Lead Sponsor
- Vice chancellor for research, Kermanshah University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 92
Inclusion Criteria
people with ages of 18 to 50 years and in good health; needing restorative treatment of maxillary premolar teeth.
Exclusion criteria: the use of anesthetic drugs and sedatives and antidepressants during two weeks before the injection; allergic reactions to local anesthetic; edentulous at the premolar region of maxilla; medical history of cardiovascular and kidney diseases; any active pathology at the injection site; gastrointestinal bleeding or ulceration; pregnant and nursing patients.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The intensity of pain. Timepoint: Immediately after the buccal and palatal injection. Method of measurement: Based on the Visual Analogue Scale (VAS).
- Secondary Outcome Measures
Name Time Method