The effect of intravenous acetaminophen in reducing Post-operative opioid requirements after maxillofacial surgery.
Phase 2
- Conditions
- Maxillofacial Surgery( correction after injury).
- Registration Number
- IRCT138711221674N1
- Lead Sponsor
- Vice chancellor for research, Shiraz University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 100
Inclusion Criteria
Inclusion Criteria: 15 to 45-year-old patients; and class I patients (ASA)
Exclusion criteria: The patients out of age range of 15 to 45 years; patients other than class I (ASA)
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Patient's hemodynamic data are evaluated in recovery room. Timepoint: 12 hours after injection of paracetamol. Method of measurement: Blood pressure and heart rate were evaluated by digital monitoring devices.;Pain of patients were measured. Timepoint: first , second, fourth, sixth, eighth, tenth, twelfth hour. Method of measurement: visual analog scale (100-mm).
- Secondary Outcome Measures
Name Time Method Patient's satisfaction. Timepoint: 12 hrs. and 24 hrs. after injection. Method of measurement: questionnaire which evaluated as poor(0), moderate(1), good(2), excellent(3).;Medication's side effects such as nausea, vomiting, gastrointestinal upset, allergic reactions, urinary retention, diarrhea, constipation was noted. Timepoint: 12 hrs. and 24 hrs. after injection. Method of measurement: Through a questionnaire that contains information about the drug side effects.