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Microvascular perfusion in renal ischemia/reperfusion injury during clinical kidney transplantation: an observational study.

Microvascular perfusion in renal ischemia/reperfusion injury during clinical kidney transplantation: an observational study. - Microvascular perfusion during kidney transplantation.

Status
Unknown
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON36643
Enrollment
80
Registered
2011-02-21
Start date
Unknown
Completion date
Unknown
Last updated
2024-05-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

ischemia/reperfusion injury Kidney transplantation

Interventions

None listed

Sponsors

Medisch Universitair Ziekenhuis Maastricht
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: - Subjects must sign the informed consent document prior to performance of any study related procedure including the Screening procedure. - Received kidney from; 1) living donor (n=12), 2)including the donor (n=12), brain-dead donor (n=12) and from donors after cardiac death (n=12). - Males and females >= 18 years of age.

Exclusion criteria

Exclusion criteria: - Smoking and a current history of smoking in the past six months. - Donor age 60 years.

Design outcomes

Primary

MeasureTime frame
Renal perfusion: 1. Renal artery flow measured by Laser-Doppler flow probe. 2. Microcirculatory perfusion measured by OPS imaging (parameters: volumetric blood flow, functional capillary density).

Secondary

MeasureTime frame
Kidney function: 1. Dialysis dependency after transplantation. 2. Area under the curve for serum creatinine concentration over time (14 days). 3. Fractional excretion of sodium (14 days). Inflammation: Serum cytokine concentrations (IFN-γ, TNF-a, IL-6, IL-10, IL-17, IL-23). Renal cellular injury: Urine NGAL and NAG concentrations. Anti-oxidants: vitamin C, vitamin E, GSH/GSSG ratio, total anti-oxidant capacity. Endothelial glycocalyx: 1. Thickness measured by OPS imaging 2. Renal arterio-venous differences in syndecan-1, heparin sulphate and hyaluronan concentrations.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)