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Contact Information:

Neeraj Dhaun bean.dhaun@ed.ac.uk


Hannah Preston, MBCHb 447889742171
v1hprest@ed.ac.uk


Study Location:

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Be Part of Research - Trial Details - MEMRI and Kidney Disease

MEMRI and Kidney Disease

Recruiting

Open to: ALL

Age: 18.0 - N/A

Medical Conditions

Kidney Diseases
Renal Insufficiency, Chronic
Acute Kidney Injury
Vasculitis


This information is provided directly by researchers, and we recognise that it isn't always easy to understand. We are working with researchers to improve the accessibility of this information. In some summaries, you may come across links to external websites. These websites will have more information to help you better understand the study.


Acute kidney injury (AKI) is common and costly.1 Although patients who suffer an episode of AKI may recover, many will go on to develop cardiovascular disease and chronic kidney disease (CKD). Cardiovascular disease is an important complication of AKI.2 Similar to AKI, CKD and kidney transplantation and kidney donation associations with cardiovascular disease.1 The risk of cardiovascular disease complications is also increased in patients with inflammatory diseases that affect the kidneys, such as vasculitis.

Currently, there are no reliable biomarkers that will identify those patients with kidney disease that will go on to develop cardiovascular disease. This study will explore the potential of manganese-enhanced magnetic resonance imaging (MEMRI) to act as a biomarker of AKI and its cardiovascular and renal complications. An analogue of calcium, manganese is readily taken-up into viable cells where it increases T1 relaxivity. Preliminary data show rapid manganese uptake in the heart and kidneys of healthy subjects.

The investigators propose to use MEMRI to demonstrate differences in renal and myocardial calcium handling in patients with acute insults (such as AKI, transplant rejection, donation or episodes of rejection or new vasculitis presentations) or improvements (such as transplantation). The investigators will also investigate whether these abnormalities reverse in those whose injury resolves or persist in those who clearly develop CKD, or who are at risk of future cardiovascular disease and CKD.

Start dates may differ between countries and research sites. The research team are responsible for keeping the information up-to-date.  

The recruitment start and end dates are as follows:

Nov 2024 Nov 2029

Publications

"Legrand M, Rossignol P. Cardiovascular Consequences of Acute Kidney Injury. N Engl J Med. 2020 Jun 4;382(23):2238-2247. doi: 10.1056/NEJMra1916393. No abstract available."; "32492305"; "Bellomo R, Kellum JA, Ronco C. Acute kidney injury. Lancet. 2012 Aug 25;380(9843):756-66. doi: 10.1016/S0140-6736(11)61454-2. Epub 2012 May 21."; "22617274"

OBSERVATIONAL

Intervention Type : DIAGNOSTIC_TEST
Intervention Description : MRI imaging of the kidney and heart with an intravenous infusion of manganese dipyridoxl diphosphate (Mangafodipir, MnDPDP).

Intervention Arm Group : Acute Kidney Injury;Chronic Kidney Disease;Control Subjects;Kidney failure undergoing transplantation;Kidney transplant rejection;Vasculitis;

Intervention Type : DIAGNOSTIC_TEST
Intervention Description : full blood count, urea and electrolytes, liver function test, CRP, biomarkers for endothelial function, storage of serum and plasma for future analyses.

Intervention Arm Group : Acute Kidney Injury;Chronic Kidney Disease;Control Subjects;Kidney failure undergoing transplantation;Kidney transplant rejection;Vasculitis;

Intervention Type : DIAGNOSTIC_TEST
Intervention Description : Urine protein, Urine creatinine

Intervention Arm Group : Acute Kidney Injury;Chronic Kidney Disease;Control Subjects;Kidney failure undergoing transplantation;Kidney transplant rejection;Vasculitis;

Intervention Type : DIAGNOSTIC_TEST
Intervention Description : 24 hour blood pressure, arterial stiffness

Intervention Arm Group : Acute Kidney Injury;Chronic Kidney Disease;Control Subjects;Kidney failure undergoing transplantation;Kidney transplant rejection;Vasculitis;



You can take part if:



You may not be able to take part if:


This is in the inclusion criteria above


Below are the locations for where you can take part in the trial. Please note that not all sites may be open.

  • NHS Lothian
    Edinburgh

Hannah Preston, MBCHb 447889742171
v1hprest@ed.ac.uk


Neeraj Dhaun bean.dhaun@ed.ac.uk



The study is sponsored by University of Edinburgh and is in collaboration with NHS Lothian.





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Read full details for Trial ID: NCT06698614
Last updated 20 November 2024

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