PAIN control after laparoscopic Surgery using EpiduRal anesthesia Versus Intravenous aCEtaminophen with local anesthesia: an open-label pilot study
Not Applicable
- Conditions
- Patients undergoing laparoscopic surgery
- Registration Number
- JPRN-UMIN000033472
- Lead Sponsor
- Wakayama Medical University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up continuing
- Sex
- All
- Target Recruitment
- 45
Inclusion Criteria
Not provided
Exclusion Criteria
1)Epidural catheter can not to be inserted technically 2)Platelet counts <= 100,000 3)Bleeding tendency 4)Patients who can not express their pain (can not use patient-controlled anesthesia) 5)Patients with severe comorbidity(heart failure, renal failure, psychiatric disorder and so on) 6)Transaminase(AST, ALT) >= twofold more than normal limits 7)Patients who took another oral analgesic within preoperative 8 hours 8)Pregnancy or breast-feeding women 9)Aspirin-induced asthma 10)active peptic ulcer 11)Patient with allergy to acetaminophen, opioid or local anesthesia 12)Others
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The amount of patient-controlled anesthesia for breakthrough analgesia at postoperative 72 hours
- Secondary Outcome Measures
Name Time Method VAS(visual analogue scale) adverse effect