New MRI technique aims to spot kidney transplant rejection early
NCT ID NCT03192007
First seen Jun 25, 2026 · Last updated Sep 17, 2026 · Updated 3 times
Summary
This study will use advanced MRI scans to look at kidney transplants in 140 patients. The goal is to see if MRI can measure how well the kidney is working and tell the difference between stable function and problems like rejection. Researchers hope this could lead to a non-invasive way to monitor transplant health, possibly reducing the need for biopsies.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Magnetic Resonance Imaging (MRI)
- What this could lead to
- If successful, MRI could become a non-invasive tool to monitor kidney transplant health and detect problems early, reducing the need for biopsies.
- What could go wrong
- This is an early pilot study focused on developing and testing MRI methods, not a treatment. It may not show clear benefits or lead to immediate changes in care.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 140 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Jul 2027
An estimate. Start dates often move.
- Expected to finish
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Dec 2028
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
The proposed studies are pilot studies to obtain preliminary data for the development of hypotheses and estimate the power for future large-scale studies. To accomplish the objectives of the proposed pilot studies, we will enroll a total of 140 renal transplant patients. Based on our previous experience, there will be about 20% patients who may withdraw after informed consent. Equal number of male and female subjects will be recruited for each patient group. In addition, the age of patients will be matched or ensured insignificant across the groups of the study objectives.
- Ages
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18 to 75 years
- Sex
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Anyone
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Renal Transplant Recipients * Capable to consent * English speaking * For studies with patients with fast worsening renal function: An abrupt (within 48 h) reduction in kidney function currently defined as a percentage increase in serum creatinine of ≥50% (1.5-fold from baseline), or a reduction in urine output (documented oliguria of less than 0.5 mL/kg/h for more than 6 h). * For patients with recovered renal allograft function after therapy: renal allograft function as measured by glomerular filtration rate (eGRF) has been recovered and stabilized above a clinical acceptable level, such as 15 ml/min/1.73 mm2. Exclusion Criteria: * On dialysis due to renal allograft failure * Acute and chronic pulmonary disease * Pregnancy as reported in CMRR Safety Screen * Ferromagnetic implants * Any foreign metal objects in the body * History of shrapnel or shot gun injury * Cardiac pacemakers * Defibrillator * Neuronal stimulator * Magnetic aneurysm clip * Large tattoos on the abdomen or the brain and neck, as determined by CMRR Safety Officer * Hip replacement * Too large to fit in the magnet (BMI \>= 40, approx.) * Severe claustrophobia
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
The full official record for this study. This one lists no contact details, but it is the first place any would appear.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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CMMR
Minneapolis, Minnesota, 55455, United States
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Other studies related to the condition(s) this trial covers.
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