Scientists investigate mysterious loin pain in kidney disease
NCT ID NCT07649538
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looks at what changes occur in the kidneys, urine, and blood when people with IgA nephropathy (IgAN) experience loin pain. Researchers will use MRI scans and lab tests to compare findings during a pain episode and when pain-free. The goal is to better understand the cause of this pain, which may help improve future care.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this study could help doctors understand why loin pain occurs in IgA nephropathy, potentially pointing toward better pain management strategies.
- What could go wrong
- This is a small, early observational study with only 40 participants, so findings may not apply to everyone with IgA nephropathy. It does not test any treatment.
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 40 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Aug 2026
An estimate. Start dates often move.
- Expected to finish
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Jun 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 study population will include adults aged 18 years or over with a renal biopsy-confirmed diagnosis of Immunoglobulin A nephropathy (IgAN) who have capacity to provide informed consent. Participants will be recruited into two cohorts. Cohort A will include participants with IgAN who experience episodic or intermittent loin pain, defined as pain occurring at least once every 6 months. Cohort B will include participants with IgAN who have no history of loin pain. Participants will be excluded if they have another renal disease, are receiving therapies that may affect immune-mediated pathways, have received a kidney transplant, are receiving dialysis, are taking part in an interventional study that may affect kidney function, or have conditions or implants that are not compatible with MRI scanning.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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: Cohort A 1. ≥18 years of age at the time of recruitment 2. IgAN diagnosis confirmed with a renal biopsy 3. Episodic/Intermittent Loin Pain (defined as pain at least once every 6 months) 4. Have the capacity to consent to the study Cohort B 1\) ≥18 years of age at the time of recruitment 2) IgAN diagnosis confirmed with a renal biopsy 3) No history of loin pain 4) Have the capacity to consent to the study Exclusion Criteria: Cohort A 1. Constant loin pain 2. Infrequent loin pain (no pain experienced in the last 6 months) 3. Inability to differentiate loin pain from back pain 4. Other renal diseases 5. Therapies that interfere with immune-mediation like steroids and complement inhibitors 6. Kidney transplant recipients 7. Current participation in an interventional study that may affect kidney function 8. Patients on dialysis 9. Patients with implants that are not MRI-safe (pacemakers, implantable defibrillators, cochlear implants, some shunts, neurostimulators, some aneurysm clips, etc.) Cohort B 1. Other renal diseases 2. Therapies that interfere with immune-mediation like steroids and complement inhibitors 3. Kidney transplant recipients 4. Current participation in an interventional study that may affect kidney function 5. Patients on dialysis 6. Patients with conditions/implants that are not MRI-compatible (claustrophobia, pacemakers, implantable defibrillators, cochlear implants, some shunts, neurostimulators, some aneurysm clips, etc.)
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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
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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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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University Hospitals of Leicester
Leicester, Leicester, LE1 7HA, United Kingdom
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Other studies related to the condition(s) this trial covers.
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