N17
Conditions
Interventions
Group 1: The prospective non-interventional monocentric observational study aims to determine the plasmaclearance of Iohexol after routine radiologic procedures due to reasons irrespective of this stu
Sponsors
Universitätsklinikum Regensburg
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: At critical care ward, Iohexol is given for a procedure irrespective of the study.
Exclusion criteria
Exclusion criteria: Any of the following while samples are being obtained: ECMO therapy, renal replacement therapy or large volume shifts (f.i. massive transfusion or large blood loss). Pregnancy.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Feasibility of measurement of renal function (mGFR) based on Iohexolclearance | — |
Secondary
| Measure | Time frame |
|---|---|
| Comparison of mGFR (based on Iohexol based) with eGFR (Creatinin/Cystacin-C based) | — |
Countries
Germany
Contacts
Public ContactAlexander Dejaco
Universitätsklinikum Regensburg
Outcome results
None listed