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Intraoperative perfusion assessment during kidney transplantation

Intraoperative perfusion assessment during kidney transplantation

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00030097
Enrollment
25
Registered
2022-09-01
Start date
2019-10-01
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

N18.5

Interventions

Group 1: visual assessment of the color after reperfusion and and doppler sonographic assessment of the kidney allograft after reperfusion intraoperatively (one measuerement) Group 2: quantitative int

Sponsors

Universitätsklinikum Mannheim
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: All patients scheduled for kidney transplantation in our center.

Exclusion criteria

Exclusion criteria: allergy to iodine or ICG, severe hepatic dysfunction, pregnancy, hyperthyroidism, pulmonary hypertension and the logistical availability of both technical tools for quantitative perfusion assessment (O2C and SPY Elite)

Design outcomes

Primary

MeasureTime frame
Delayed graft function (DGF), defined as 2 or more postoperative dialysis sessions within the hospital stay

Secondary

MeasureTime frame
parameters of postoperative transplant function

Countries

Germany

Contacts

Public ContactAndreas Gerken

Universitätsmedizin Mannheim, Chirurgische Klinik

andreas.gerken@umm.de0621 383 2225

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026