Comparison of intraoperative administration of ketorolac with morphine in pain control and postoperative nausea and vomiting in patients undergoing rhinoplasty
Phase 2
Recruiting
- Conditions
- Rhinoplasty surgery.General- and plastic-surgery devices associated with adverse incidents
- Registration Number
- IRCT20210415050976N8
- Lead Sponsor
- Jahrom University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 114
Inclusion Criteria
Rhinoplasty under general anesthesia
No history of allergy to morphine and ketorolac
Exclusion Criteria
Drug addiction
Underlying cardiovascular disease
Patients with coagulation disorders or platelets less than one hundred thousand
Patients with a history of renal insufficiency and serum creatinine more than one and a half
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The pain. Timepoint: Periods immediately after surgery, 15 minutes, 3 hours and 6 hours after surgery. Method of measurement: VAS criteria.;Nausea and vomiting. Timepoint: After surgery. Method of measurement: Nausea and vomiting questionnaire.
- Secondary Outcome Measures
Name Time Method Vital signs. Timepoint: Immediately after surgery and then at 15, 3 and 6 minutes after surgery. Method of measurement: monitoring.