living donor renal transplantation
Conditions
Interventions
After the induction of general anesthesia, Carperitide or placebo drug(normal saline) was intravenously administrated at a rate of 0.025mcg/kg/min. We measured urinary liver-type fatty acid binding pr
Sponsors
Toho University School of Medicine, Department of Anesthesiology
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Patients with written informed consent
Exclusion criteria
Exclusion criteria: Patients without written informed consent
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The concentrations of urinary liver-type fatty acid binding protein after renal transplantation. | — |
Countries
Japan
Contacts
Public ContactRikizo Kogawa
Toho University School of Medicine Department of Anesthesiology
Outcome results
None listed