HD-REMODEL: HaemoDialysis Interventions to REduce Multi-Organ Dysfunction and Effect on Quality of Life Assessed by MRI Scanning
Study Details
Study Description
Brief Summary
The purpose of this study is to characterise in detail cardiac, cerebral and renal structure, function and perfusion in patients on haemodialysis (HD) using magnetic imaging techniques. The effects of a standard prescription haemodialysis (dialysate temperature 37 C) will be compared to a thermocontrolled (or isothermic) haemodialysis prescription to ascertain if thermocontrolled HD provides a protective effect on organ perfusion and circulatory stress when compared to conventional haemodialysis. The BTM (blood temperature monitor, Fresenius) offers a way to overcome this to regulate thermal balance during dialysis and achieve a neutral thermal balance (isothermic) over the dialysis session. Other dialysis parameters will be standardised between treatment arms using blood volume monitoring (BVM) and clinical assessments.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
N/A |
Detailed Description
The purpose of this study is to characterise in detail cardiac, cerebral and renal structure, function and perfusion in patients on haemodialysis (HD) using magnetic imaging techniques. The Primary objectives are to investigate the difference in cardiac perfusion, structure and function between standard HD and thermocontrolled HD using magnetic imaging techniques, to observe the the changes in renal perfusion and oxygenation within one dialysis session and the changes to cerebral perfusion within one dialysis session.
The secondary objectives are to investigate the difference in cerebral perfusion, structure, oedema and function between standard HD and thermocontrolled HD, the difference in renal perfusion and oxygenation between standard HD and thermocontrolled HD and the differences in visual acuity and cognitive assessment across a dialysis session and over a dialysis treatment course.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Experimental: Standard HD HD with constant temperature of 37°C, MRI scans of the heart, kidneys and brain during HD sessions |
Other: HD, Magnetic Resonance Imaging (MRI) scans
HD, Magnetic Resonance Imaging (MRI) scans using a specifically designed unit able to perform MRI scanning during HD sessions
|
| Experimental: Thermocontrolled HD HD applying the Blood Temperature Monitor (BTM), MRI scans of the heart, kidneys and brain during HD sessions |
Other: HD, Magnetic Resonance Imaging (MRI) scans
HD, Magnetic Resonance Imaging (MRI) scans using a specifically designed unit able to perform MRI scanning during HD sessions
|
Outcome Measures
Primary Outcome Measures
- Change in cardiac output during standard HD and thermocontrolled HD [after 2 and 4 weeks after randomisation]
Change in cardiac output during standard HD and thermocontrolled HD using Phase Contrast Magnetic Resonance Imaging (PC-MRI)
- Change in renal perfusion during standard HD and thermocontrolled HD [after 2 and 4 weeks after randomisation]
Change in renal perfusion using Arterial Spin Labelling (ASL) and renal artery flow using PC-MRI
- Change in cerebral perfusion during standard HD and thermocontrolled HD [after 2 and 4 weeks after randomisation]
Change in cerebral perfusion during standard HD and thermocontrolled HD using ASL
Eligibility Criteria
Criteria
Exclusion Criteria:
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Change in dry weight (clinically defined) in 4 weeks prior to recruitment
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Dialysate composition other than: sodium≥137mmol/L, potassium≥2.0mmol/L, calcium≥1.5mmol/L, magnesium≥0.5mmol/L, glucose 1.0g/L
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Instability on dialysis in 4 weeks prior to recruitment leading to either:
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Emergency medical attention
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Infusion of additional fluid
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Loss in consciousness
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Arrhythmia
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Chest pain
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Or any other medical condition that precludes the scan session in opinion of the investigator
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Dialysed via a synthetic line, central venous catheter or graft
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Qa < 500ml/min
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NYHA Stage IV heart failure (New York Heart Association)
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Active infection or malignancy
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Contraindication to MRI scanning including claustrophobia, pacemaker, metallic implants etc
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Pregnancy (pregnancy test will be conducted with female patients aged ≤ 55 years) or planning pregnancy or lactation period
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Medical conditions or overall physical frailty precludes scan session in opinion of investigator
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Unable or unwilling to provide informed consent
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Any condition which could interfere with the patient's ability to comply with the study
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Participation in an interventional clinical study during the preceding 30 days
Inclusion Criteria:
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Age 18-80, male and female
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Informed consent signed and dated by study patient and investigator/authorised physician
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Average (4 weeks prior to recruitment) Ultrafiltration volumes ≥ 0.5 litres/ dialysis session
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Receiving dialysis via an arteriovenous fistula
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Must be able to follow simple instruction in English (on safety grounds for MRI scans) and be able to understand the nature and requirements of the study
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Stable dialysis prescription
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CKD5 (Chronic kidney disease) patients having renal replacement therapy with haemodialysis/ haemodiafiltration (>90 days)
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | University of Nottingham, Division of Medical Sciences and Graduate Entry Medicine | Nottingham | United Kingdom |
Sponsors and Collaborators
- Fresenius Medical Care Deutschland GmbH
Investigators
- Study Chair: Maarten Taal, Professor, University of Nottingham, Division of Medical Sciences and Graduate Entry Medicine
- Principal Investigator: Nicolas Selby, Dr, University of Nottingham, Division of Medical Sciences and Graduate Entry Medicine
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- HD-Remodel-UK-01
- IRAS 207142