Analgesic effect of peripheral nerve block after gynecological lower abdominal surgery; concentration versus volume of local anesthetic.A prospective randomized trial.
Not Applicable
- Conditions
- Patients who are scheduled for gynecological lower abdominal surgery.
- Registration Number
- JPRN-UMIN000019766
- Lead Sponsor
- agoya University Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- Female
- Target Recruitment
- 48
Inclusion Criteria
Not provided
Exclusion Criteria
1)Patients who have stomach ulcer, renal failure or liver failure. 2)Patients who have allergy to the drugs which will going to use in this trial. 3)Patients who have severe obesity over BMI 30. 4)Patients who have contraindication of Ropivacaine. 5)Patients who are regarded ineligible by doctors with ather reasons.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Postoperative morphine consumption after 4, 24, 48, and 72 hours.Using patient controlled analgesia.
- Secondary Outcome Measures
Name Time Method Pain:Visual analogue scale(VAS) at rest and at cough after 4, 24, 48, and 72 hours postoperation. Adverse event. Blood pressure and SpOs after 4,24,48 and 72 hours postoperation, Ropivacaine plasma concentration after 0,15,30,45,60 and 120 mins after transversus abdominis plane block.