N17.9
Conditions
Interventions
Group 1: This trial intends to enable physicans to predict kidney injury due to aortic surgery (via laparotomy or endovascular) at an early stage. This would allow early identificaton of risk patients
Sponsors
Klinik für Anästhesiologie
Eligibility
Sex/Gender
All
Age
18 Years to 108 Years
Inclusion criteria
Inclusion criteria: aortic surgery (via laparotomy or endovascular)
Exclusion criteria
Exclusion criteria: - not fulfilling the inclusion criteria - not able to give writen informed consent - not willing to participate
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| For the prediction of a moderate or severe acute kidney injury blood and urine samples will be collected immediately before and after the surgical procedure, as well as at the first postoperative day. Standard laboratory and G1-cellcycle Arrest biomarker “insulin like growth factor binding protein-7” (IGFBP-7) and “tissue inhibitor of metalloproteinase-2” (TIMP-2) will be measured. IGFBP-7 and TIMP-2 Levels will be measured by a Point of care device in Urine samples. The standard laboratory markers (e.g. creatinine) will be measured in plasma samples at the central lab (University Hospital Heidelberg). | — |
Secondary
| Measure | Time frame |
|---|---|
| Association between IGFBP-7xTIMP-2 urine concentrations and the kidney function immediately after the surgical procedure and at the first postoperative day. | — |
Countries
Germany
Contacts
Public ContactThorsten Brenner
Klinik für Anästhesiologie
Outcome results
None listed