TCTR20200512002Recruiting未知
Effect of Intravenous Acetaminophen on Postoperative Morphine Consumption in Benign Open Abdominal Gynecological Surgeries: A double-blind, randomized, placebo-controlled trial
Faculty of Medicine, Chiang Mai University0 sites100 target enrollmentStarted: May 12, 2020Last updated:
Conditions
Trial Snapshot
- Phase
- 未知
- Status
- Recruiting
- Sponsor
- Enrollment
- 100
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
Eligibility Criteria
- Ages
- 18 Years to 65 Years (—)
- Sex
- Female
Inclusion Criteria
- •1.Women aged 18-65 years old
- •2.Patients who undergoing elective benign open abdominal gynecological surgery
- •3.American Society of Anesthesiologists (ASA) Class I-III
Exclusion Criteria
- •1.Patients with known allergy to acetaminophen, parecoxib, sulfonamides, aspirin or opioids
- •2.Patients with either acute or chronic liver disease (defined as abnormal rising AST ALT, hypoalbuminemia, prolonged INR, or evidence from imaging diagnosis)
- •3.Patients with moderate to severe pain before surgery
- •4.Third trimester pregnant patients or lactation period
- •5.Patients receive any additional neuraxial block or peripheral nerve blocks for pain control
- •6.Patients with history of opioid abuse or chronic opioid use for greater than 3 months
- •7.Patients with suspected malignant gynecological disease intraoperatively and undergo extended lymph node dissection or complete surgical staging
- •8.Patients with contraindication to parecoxib (post CABG surgery, established ischemic heart disease, peripheral arterial disease and/or cerebrovascular disease, inflammatory bowel disease, Child-Pugh score ≥ 10, active peptic ulcer/ GI bleeding, known hypersensitivity to sulfonamides)
Investigators
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