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Renal Physiology During Continuous Renal Replacement Therapy

S

Sahlgrenska University Hospital

Status

Enrolling

Conditions

AKI
Renal Failure
Dialysis
Renal Blood Flow
Continuous Renal Replacement Therapy
Blood Pressure
Intensive Care

Treatments

Other: Starting at high or low blood pressure

Study type

Interventional

Funder types

Other

Identifiers

NCT04114747
Kidney and dialysis

Details and patient eligibility

About

Approximately 50% of patients in the intensive care unit (ICU) develop acute kidney injury (AKI) and more than 10% need dialysis. There is no treatment for AKI. Care is aiming for optimization of circulation and blood flow to the kidneys and avoiding nephrotoxic agents.

There is conflicting data concerning whether early or late dialysis is harmful for the kidneys. No one has examined the physiological changes in the kidney when starting dialysis and which blood pressure that leads to most optimal physiological conditions for the kidneys during dialysis. In this descriptive study of 20 ICU patients suffering from AKI we aim to investigate renal physiology when starting continuous renal replacement therapy (CRRT) and also at different target blood pressures using retrograde renal vein thermodilution technique. In parallel we will also investigate and validate this invasive method with contrast enhanced ultrasound of the kidneys.

Enrollment

20 estimated patients

Sex

All

Ages

18 to 90 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

AKI, according to KDIGO, stage 2 or 3 but with preserved urine production. Treated in the ICU at Sahlgrenska University Hospital Written, signed informed consent Male and female subjects ≥18 years

Exclusion criteria

Emergency need for dialysis Allergy to contrast media (used for CEUS)

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

20 participants in 2 patient groups

Starting at high blood pressure
Experimental group
Description:
Patients in this arm are randomized to have high target blood pressure at MAP 80-90 mmHg during the first recordings, thereafter they will receive low blood pressure target 60-70 mm Hg
Treatment:
Other: Starting at high or low blood pressure
Starting at low blood pressure
Experimental group
Description:
Patients in this arm are randomized to have low target blood pressure at MAP 60-70 mmHg during the first recordings, thereafter they will receive high blood pressure target 80-90 mm Hg
Treatment:
Other: Starting at high or low blood pressure

Trial contacts and locations

1

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Central trial contact

Kristina Svennerholm, MD PhD; Christian Rylander, MD PhD

Data sourced from clinicaltrials.gov

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