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NCT06174610
Changes of Renal Resistive Index in Critically Ill Patients Undergoing Continuous Renal Replacement Therapy.
trial testing Measurement of Renal Resistive Index in Acute Kidney Injury in 50 participants. Currently enrolling.
21 May 2026
Quick facts
| Lead sponsor | Uniwersytecki Szpital Kliniczny w Opolu |
|---|---|
| Status | Recruiting now |
| Study type | OBSERVATIONAL |
| Enrollment | 50 |
| Start date | 19 December 2023 |
| Primary completion | 21 May 2026 |
| Estimated completion | 18 December 2026 |
| Sites | 1 location across Poland |
Drugs / interventions tested
- Measurement of Renal Resistive Index
Conditions studied
- Acute Kidney Injury — all drugs for Acute Kidney Injury →
Sponsor
Uniwersytecki Szpital Kliniczny w Opolu — full company profile →
Who can join
18 and older, any sex, with Acute Kidney Injury. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
The aim of the study is to determine whether there is a correlation between changes in the renal resistive index and the restoration of kidney function in critically ill patients undergoing continuous renal replacement therapy.
Publications & conference data
No peer-reviewed publications indexed yet for this trial.
Verify or expand the search:
- PubMed search for NCT06174610
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other recruiting trials for Acute Kidney Injury
Currently open trials in the same condition.
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- NCT07262320 — Epidemiology and Processes of Care for Renal Replacement Therapy in Acute Kidney Injury in Latin America · recruiting
- NCT07351149 — Postoperative Acute Kidney Injury in Children Undergoing Major Non-cardiac Surgery · recruiting
- NCT07215702 — A Study to Investigate the Efficacy, Safety, and Tolerability of AZD4144in Participants With Sepsis-associated Acute Kid · Phase 2 · recruiting
- NCT06654193 — Allogeneic HB-adMSCs vs Placebo for the Treatment of Acute Kidney Injury · Phase 1, PHASE2 · recruiting
Other Uniwersytecki Szpital Kliniczny w Opolu trials
Trials by the same sponsor.
- NCT06188039 — Superior Vena Cava Collapsibility Index for Predicting Fluid Responsiveness During High-risk Non-cardiac Surgery · NA · completed
- NCT06729268 — Fluid Responsiveness Tests in Critically Ill Patients During Admission to the Intensive Care Unit · completed
- NCT05657678 — Vitamin D3 Supplementation in Critically Ill Patients Undergoing CRRT · Phase 4 · recruiting
- NCT03412422 — Ultrasound Assessment of Changes in the Diameter of the Common Carotid Artery After Increasing the Preload of the Heart · withdrawn
- NCT03873675 — Parathyroid Hormone Kinetics During CRRT · completed
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT06174610 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Uniwersytecki Szpital Kliniczny w Opolu
- Last refreshed: 3 June 2025
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06174610.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing