Patients who are scheduled for gynecological lower abdominal surgery.
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1)Patients who are scheduled for gynecological lower abdominal surgery in Nagoya university hospital. 2)American Society of Anethesiologists physical status in 1, 2 or 3. 3)Patients who can evaluate the pain using visual analogue scale(VAS) 4)Patients who can give written informed consent,
Exclusion criteria
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.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Postoperative morphine consumption after 4, 24, 48, and 72 hours.Using patient controlled analgesia. | — |
Secondary
| Measure | Time frame |
|---|---|
| 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. | — |
Countries
Japan
Contacts
Nagoya University Hospital Department of Anethesiology