Fixed regimen analgesic use compared with regimen if needed for pain after gum surgery: a randomized controlled trial
Phase 3
- Conditions
- Dental AssistantsDentistryM01.526.485.067.105.250
- Registration Number
- RBR-7wv259
- Lead Sponsor
- niversidade Federal do Rio Grande do Sul
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Data analysis completed
- Sex
- Not specified
- Target Recruitment
- Not specified
Inclusion Criteria
Adult patients; Patients of both sexes; Patients in need of periodontal surgery with total flap to restore supracrystal insertion tissues.
Exclusion Criteria
Patients who use systemic analgesics; patients who use systemic antimicrobial, patients who use systemic anti-inflammatory drugs; patients who use systemic muscle relaxants; patients on systemic anxiolytic or antidepressant use; patients with previous chronic or acute pain, related or not to the oral cavity; patients who have difficulty understanding instructions (cognitive changes), impairing the application of the scales proposed by the research.
Study & Design
- Study Type
- Intervention
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Postoperative pain assessed by the Visual Analog Scale, Numerical Scale and Verbal Pain Scale 2, 6, 12, 24 and 48 hours immediately after surgery.
- Secondary Outcome Measures
Name Time Method Amount of acetaminophen consumed by the demand group and amount of rescue medication consumed by the test and control groups within 48 hours.;Preoperative anxiety level measured by the IDATE - traço e Estado scales and dental anxiety level measured by the Corah Scale.