congestive nephropathy N17.8 N18.8 N19
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: -Kidney disease with indication for kidney biopsy -voluntary participation, ability to give informed consent -Signed informed consent for this study -Legal age
Exclusion criteria
Exclusion criteria: - Refusal of the examination/participation in the study - Lack of possibility to cooperate with the sonography - Underage - Pregnancy or breastfeeding - Patients after kidney transplantation (NTX) - Circumstances that do not allow Doppler sonography to be performed or interpreted (e.g. severe dys-/tachypnea)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary endpoint is the change in duplex sonographic renal congestion parameters* after volume administration in this patient population. The parameters are measured directly before renal biopsy and directly after volume administration (as standard of care) after renal biopsy. This is done using duplex sonography (ultrasound examination). *Duplex sonographic renal congestion parameters: Here, continuous venous flow (no congestion) can be distinguished from the discontinuous flow patterns pulsatile (mild), biphasic (moderate) and monophasic (severe congestion). The venous impedance index (VII) and the renal venous stasis index (RVSI) are additional duplex sonographic criteria for detecting renal congestion, each of which approaches the value 1 as the degree of congestion increases. | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. prevalence of renal congestion in this patient population 2. correlation of renal congestion with underlying disease (e.g. nephrotic vs. non-nephrotic underlying disease) 3. correlation of renal congestion with histopathological parameters (e.g. dilated veins/tubular capillaries) 4. correlation of renal congestion with urinary proteome and metabolome 5. correlation of renal congestion with tissue proteome | — |
Countries
Germany
Contacts
Universitätsmedizin Göttingen