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Assessment of Renal Function by Multiparametric MRI

Assessment of Renal Function by Multiparametric MRI

Status
Completed
Phases
Early Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06407375
Enrollment
46
Registered
2024-05-09
Start date
2023-07-25
Completion date
2025-05-09
Last updated
2025-12-09

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

Conditions

Renal Impairment

Brief summary

Metabolic syndrome is a collection of conditions that affect at least three of the following five criteria: abdominal obesity, high blood pressure, high fasting glucose levels, high triglyceride levels, and low levels of high-density lipoprotein (HDL) cholesterol. Chronic kidney disease (CKD) is a common complication of metabolic syndrome, with an estimated prevalence of 13-40%. Early diagnosis of progressive conditions before the onset of reduced glomerular filtration rate (GFR) or albuminuria may be of clinical benefit but is not possible at present. Furthermore, the diagnosis and quantification of CKD in the context of metabolic syndrome is challenging due to the lack of reliable diagnostic biomarkers, and the current methods may not accurately reflect kidney function in patients with metabolic syndrome. Magnetic resonance imaging (MRI) has been sparsely explored as a potential tool to assess renal perfusion, oxygenation, and fibrosis. Multiparametric MRI (mpMRI) combines several different imaging techniques to provide a more comprehensive evaluation of tissue structure and function. These techniques hold promise for non-invasive assessment of kidney function, but their clinical utility is still largely experimental. Therefore, we aim to conduct an exploratory study to investigate the reliability, reproducibility as well as the validity of parameters for kidney function of multiparametric MRI as well as compare these parameters in between healthy patients and patients with metabolic syndrome.

Interventions

DIAGNOSTIC_TESTmpMRI

mpMRI

Sponsors

University of Zurich
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Diagnosed metabolic syndrome

Exclusion criteria

* MRI

Design outcomes

Primary

MeasureTime frameDescription
T1 Time6 monthsT1 relaxation time (MR characteristic of the human tissue, measured in ms)

Countries

Switzerland

Participant flow

Participants by arm

ArmCount
Healthy Participants
Healthy participants of different age groups
46
Total46

Baseline characteristics

CharacteristicHealthy Participants
Age, Categorical
<=18 years
0 Participants
Age, Categorical
>=65 years
0 Participants
Age, Categorical
Between 18 and 65 years
46 Participants
Race and Ethnicity Not Collected— Participants
Serum Creatinine72 µmol/L
STANDARD_DEVIATION 14.4
Sex: Female, Male
Female
25 Participants
Sex: Female, Male
Male
21 Participants

Adverse events

Event typeEG000
affected / at risk
deaths
Total, all-cause mortality
0 / 46
other
Total, other adverse events
0 / 46
serious
Total, serious adverse events
0 / 46

Outcome results

Primary

T1 Time

T1 relaxation time (MR characteristic of the human tissue, measured in ms)

Time frame: 6 months

ArmMeasureValue (MEAN)Dispersion
Healthy participantsT1 Time1500 msStandard Deviation 15

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026