Comparison of the effects of dexketoprofen application before the operation or before the end of the operation on postoperative pain in nasal surgery.
Phase 4
Completed
- Conditions
- postoperative analgesiaAnaesthesiology - Pain managementAnaesthesiology - Anaesthetics
- Registration Number
- ACTRN12612000317897
- Lead Sponsor
- Firat University Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- All
- Target Recruitment
- 100
Inclusion Criteria
ASA status I-II,
18-60 years old,
scheduled for septorhinoplasty
Exclusion Criteria
Patients with known heart, kidney, liver and hematological diseases, peptic ulcer and gastrointestinal bleeding, with allergic reaction to non-steroid anti-inflammatory drugs and chronic pain history and those who received analgesics in the last 24 hours were excluded into the study.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method pain assesment with Visuel Analog scale (VAS)[1, 2, 3, 4, 5, 6, 7, 8, 12 and 24 hours];intraoperative analgesic consumption[after recovery from anesthesia];postoperative analgesic consumption[postoperative 24 hours]
- Secondary Outcome Measures
Name Time Method Sedation score[1, 2, 3, 4, 5, 6, 7, 8, 12 and 24 hours];The patient satisfaction in 24 hours was evaluated according to the following 5 point scale; 1: very satisfied, 2: satisfied, 3: neither satisfied nor unsatisfied, 4: unsatisfied and 5: very unsatisfied.[postoperative 24 hours];Postoperative nausea and vomiting was classified by using the following numerical scoring system, 0: no nausea or vomiting, 1: only nausea, 2: vomiting once in 30 minutes, 3: vomiting twice or more in 30 minutes. Patients with a nausea and vomiting score of 3 or the ones that have persistent nausea for more than two hours were assessed as severe nausea and vomiting and were administered 150 mg/kg metoclopramide intravenously[1, 2, 3, 4, 5, 6, 7, 8, 12 and 24 hours]