Clinical trial Recruiting at 1 site Observational Ages 18 and up

Measuring kidney blood flow changes in critically ill patients on dialysis.

Official title: Changes of Renal Resistive Index in Critically Ill Patients Undergoing Continuous Renal Replacement Therapy - Observational Study.

Run by Uniwersytecki Szpital Kliniczny w Opolu · NCT06174610 · Data updated 2026-11-12

This study is testing if measuring kidney blood flow changes can help doctors spot kidney problems earlier in critically ill patients on dialysis.

Quick facts

Study typeObservational
Ages18 Years and up
SexAll
Enrollment50 (estimated)
SponsorUniwersytecki Szpital Kliniczny w Opolu
Academic / other
Locations1 site (Opole, Opole Voivodeship)
StatusRecruiting
StartedDecember 19, 2023
Main results expectedMay 21, 2026
Study endsDecember 18, 2026
Registry record updatedJune 3, 2025
Trial IDNCT06174610 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates for this study are ICU patients who are undergoing continuous renal replacement therapy due to acute kidney injury.

Probably not a fit

Patients under 18 years old, pregnant women, or those with severe chronic kidney disease or other specific conditions that hinder reliable RRI measurement will not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study aims to explore the relationship between changes in the renal resistive index (RRI) and the recovery of kidney function in critically ill patients undergoing continuous renal replacement therapy (CRRT) for acute kidney injury (AKI). By utilizing Doppler ultrasound measurements to assess RRI, the study seeks to identify earlier indicators of kidney dysfunction compared to traditional markers like serum creatinine. The findings could enhance monitoring strategies for AKI in intensive care settings, potentially improving patient outcomes.

Why it matters

Potential benefit: If successful, this study could lead to earlier detection and intervention for acute kidney injury, improving recovery rates in critically ill patients.

How similar studies have gone: Previous studies have shown a correlation between renal resistive index and acute kidney injury, suggesting that this approach may be promising but is still being explored.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* All ICU patients undergoing CRRT due to AKI

Exclusion Criteria:

* age \<18 years
* pregnancy
* history of chronic kidney disease in stage 4 or 5
* post-kidney transplant status
* mechanical circulatory support
* occurrence of one or more conditions preventing reliable RRI measurement in both kidneys:

  * challenging technical conditions of ultrasound examination, hindering proper visualization of the kidney
  * post-kidney injury in grade III and higher, according to AAST
  * advanced parenchymal kidney pathology: atrophy, hypoplasia, cirrhosis, extensive ischemia (more than 2/3 of the parenchyma),
  * kidney diseases preventing parenchyma identification: advanced cancer (stage above T1 according to TNM), certain forms of polycystic kidney disease
  * inflammatory kidney diseases
  * obstructive uropathy
  * renal vascular pathologies: renal vein thrombosis, significant stenosis (\>60%), and renal artery occlusion.

Where it's running

  • Department of Anesthesiology and Intensive Care, Uniwersytecki Szpital Kliniczny w Opolu
    Opole, Opole Voivodeship, Poland
    Recruiting

Similar studies

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.