Assessment of the postoperative analgesic efficacy of periodic intravenous administration of acetaminophen after gynecologic laparoscopic surgery
Not Applicable
- Conditions
- uterine disease
- Registration Number
- JPRN-UMIN000038175
- Lead Sponsor
- ippon Life Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- Female
- Target Recruitment
- 129
Inclusion Criteria
Not provided
Exclusion Criteria
1)Patients who weigh less than 40 kg and over 100 kg 2)Pregnant patients 3)Patients with nervous, heart, respiratory complications 4)Patients with allergy to acetaminophen, opioid and local anesthetics 5)Patients taking antipsychotics 6)Patients with liver and renal dysfunction 7)Patients who cannot understand pain scale 8)Patients who cannot obtain agreements 9)Patients who need additional open incision
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Frequency of supplemental or rescue analgesic administration for 24 hours postoperatively
- Secondary Outcome Measures
Name Time Method 1)the pain score (numerical rating scale: NRS) at rest at 6, 12 and 24 hours postoperatively 2)satisfaction of the patient at 24 hours postoperatively 3)frequency of nausea and vomiting for 24 hours postoperatively 4)frequency of antiemetic administration for 24 hours postoperatively