Kidney Diseases Clinical Trial
Official title:
Validation of Contrast Enhanced Ultrasound (CEUS) for the Assessment of Renal Perfusion Using Renal Magnetic Resonance Imaging (MRI), and Its Application in Acute Kidney Injury (AKI)
The purposes of this study is 1. To establish the validity of CEUS to measure renal perfusion by comparing it against ASL-MRI in young and older healthy volunteers, and generate a normative dataset of CEUS measures of renal perfusion. 2. Establish proof of principle for the use of CEUS to measure renal perfusion in the acute phase of AKI, demonstrating its feasibility and potential clinical utility. We will do this by performing daily CEUS measurements for up to five days in a cohort of people with AKI stage 3, commencing as close to onset. of AKI as possible, correlating with clinical data and following outcomes until 90 days.
Status | Not yet recruiting |
Enrollment | 50 |
Est. completion date | April 2023 |
Est. primary completion date | April 2023 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years to 70 Years |
Eligibility | Stage1(healthy volunteers) Inclusion Criteria: - Healthy male or female aged 18 years or older and able to give informed, written consent. Exclusion Criteria: - estimated Globular Filtration Rate (eGFR) <60ml/min or albuminuria - Diabetes - Prescription of anti-hypertensive agents that alter renal haemodynamics (renal angiotensin - Known allergy to SonoVue contrast agent - Contraindications to MRI Stage2 (AKI group): Inclusion criteria: AKI stage 3 (as per KDIGO criteria). Exclusion criteria: - autosomal dominant polycystic kidney disease - glomerulonephritis receiving immunosuppression - multiple myeloma - obstructive uropathy - solid organ transplant - known allergy to Sonvue - lack of baseline serum creatinine value within previous 365 days ->72hrs elapsed since detection of AKI |
Country | Name | City | State |
---|---|---|---|
United Kingdom | University of Nottingham | Derby |
Lead Sponsor | Collaborator |
---|---|
University of Nottingham |
United Kingdom,
Arthuis CJ, Mendes V, Même S, Même W, Rousselot C, Winer N, Novell A, Perrotin F. Comparative determination of placental perfusion by magnetic resonance imaging and contrast-enhanced ultrasound in a murine model of intrauterine growth restriction. Placenta. 2018 Sep;69:74-81. doi: 10.1016/j.placenta.2018.07.009. Epub 2018 Jul 18. — View Citation
Cox EF, Buchanan CE, Bradley CR, Prestwich B, Mahmoud H, Taal M, Selby NM, Francis ST. Multiparametric Renal Magnetic Resonance Imaging: Validation, Interventions, and Alterations in Chronic Kidney Disease. Front Physiol. 2017 Sep 14;8:696. doi: 10.3389/fphys.2017.00696. eCollection 2017. — View Citation
Heinink TP, Read DJ, Mitchell WK, Bhalla A, Lund JN, Phillips BE, Williams JP. Oesophageal Doppler guided optimization of cardiac output does not increase visceral microvascular blood flow in healthy volunteers. Clin Physiol Funct Imaging. 2018 Mar;38(2):213-219. doi: 10.1111/cpf.12401. Epub 2017 Feb 6. — View Citation
Hulley SB, Cummings SR, Browner WS, Grady D, Newman TB. Designing clinical research : an epidemiologic approach. 4th ed ed. Philadelphia, PA: Lippincott Williams & Wilkins; 2013.
Liss P, Cox EF, Eckerbom P, Francis ST. Imaging of intrarenal haemodynamics and oxygen metabolism. Clin Exp Pharmacol Physiol. 2013 Feb;40(2):158-67. doi: 10.1111/1440-1681.12042. Review. — View Citation
Odudu A, Nery F, Harteveld AA, Evans RG, Pendse D, Buchanan CE, Francis ST, Fernández-Seara MA. Arterial spin labelling MRI to measure renal perfusion: a systematic review and statement paper. Nephrol Dial Transplant. 2018 Sep 1;33(suppl_2):ii15-ii21. doi: 10.1093/ndt/gfy180. — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Correlation between ASL-MRI and CEUS measures of renal perfusion | The primary outcome will be the correlation between ASL-MRI measures of cortical perfusion (ml/ 100g/min) and CEUS measures of renal microvascular blood flow. | one week, ideally 1 day. | |
Primary | Renal blood flow in AKI patients | The primary outcome will be the mean and SD or median and IQR for renal microvascular blood flow on first assessment <72h after onset of AKI as assessed by CEUS. | up to 3 months | |
Secondary | CEUS Repeatability | Intra-individual reproducibility of the CEUS measures will be assessed by taking at least two measures in each individual to calculate coefficient of variation. | 1 day | |
Secondary | Correlation between global perfusion from PC-MRI corrected flow measures and CEUS | Correlation between global perfusion from Phase contrast magnetic resonance Imaging corrected flow measures and CEUS | 1 week | |
Secondary | Correlation between kinetic time-intensity parameters of CEUS and time-resolved MRA | Correlation between kinetic time-intensity parameters of CEUS and time-resolved Magnetic Resonance Angiography | 1 week | |
Secondary | Comparison of CEUS measures with daily serum creatinine (severity and recovery of AKI) | Comparison of CEUS measures with daily serum creatinine (severity and recovery of AKI) renal recovery at day 90. | up to 3 months | |
Secondary | Nadir CEUS measures of renal microvascular blood flow in those with and without complete renal recovery at day 90. | Nadir CEUS measures of renal microvascular blood flow in those with and without complete renal recovery at day 90. | up to 3 months | |
Secondary | Relationship of CEUS measures with clinical measures. | Relationship of CEUS measures with clinical measures including blood pressure, urine output. | up to 3 months |
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