Patients who are scheduled for renal transplant from living donor
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Patients who are scheduled for renal transplant from living donor in Osaka University Hospital 2. Patients who may receive anticoagulantion and cannot receive epidural anesthesia 3. Patients who can give written informed consent
Exclusion criteria
Exclusion criteria: 1. Patinets who are allergic to any medication used in the study 2. Pantients who have abdominal pain before surgery or use analgetic drugs for chronic pain 3. Patients who have severe paralysis or severe neurologic disease 4. Patients who are regarded ineligible by doctors with any other reasons
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Cumulative fentanyl consumption in 48hours postoperation | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. Visual Analogue Scale (VAS) pain scores at rest and at mobilization after 4, 16, 24, 40 and 48hours postoperation. 2. Incidence of nausea and vomitting | — |
Countries
Japan
Contacts
Graduate School of Medicine, Osaka University Department of Anesthesiology and Intensive Care Medicine