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Renal Functional Imaging for Non-invasive Evaluation and Diagnostics

Renal Functional Imaging for Non-invasive Evaluation and Diagnostics - ReFINED

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON45267
Enrollment
35
Registered
2018-03-06
Start date
2020-03-05
Completion date
Unknown
Last updated
2024-02-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

hypertensie chronic kidney disease loss of kidney function

Interventions

Functional MRI
Inulin clearance
Kidneys
Renal function

Sponsors

Universitair Medisch Centrum Utrecht
Lead Sponsor

Eligibility

Age
18 Years to 64 Years

Inclusion criteria

Inclusion criteria: - Subject is >= 18 years of age - Subject agrees to have all study procedures performed, and is competent and willing to provide written, informed consent to participate in this clinical study;Exclusively for subjects in the CKD group: - Subject has a GFR of 30-60 ml/min/1.73 m2 ;Exclusively for subjects in the hypertension group: - Subject has a systolic blood pressure of >=140 mmHg and/or a diastolic blood pressure of >=90 mmHg based on average of 3 office blood pressure readings, or a 24-h ambulatory blood pressure of >=140 mmHg systolic and/or >=90 mmHg diastolic; or is on antihypertensive medication - Subject has no treatable secondary cause of hypertension - Subject has no medical record of impaired kidney function (as defined by a GFR =140 mmHg and/or a diastolic blood pressure of >=90; or the use of antihypertensive medication) - Subject can be age matched within a range of ±5 years to one or more subjects in the CKD and hypertension groups

Exclusion criteria

Exclusion criteria: - Subject has an allergy or intolerance to any of the agents used in the study - Subject has any contraindications for MRI according to screening protocol radiology department UMCU - Subject is pregnant, nursing or planning to be pregnant - Subject has a known, unresolved history of drug use or alcohol dependency, lacks the ability to comprehend or follow instructions, or would be unlikely or unable to comply with study follow-up requirements - Subject refuses to be informed of chance findings possibly relevant to their health - Subject is currently being treated with drugs that cause salt retention (e.g., systemic corticosteroids and fludrocortisone);Exclusively for healthy volunteers and hypertensive subjects: - Subject has no known renal disease

Design outcomes

Primary

MeasureTime frame
Agreement between GFR as measured with MRI and GFR as measured with inulin clearance.

Countries

The Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)