Can a massive kidney database unlock IgA Nephropathy's secrets?
NCT ID NCT04858724
First seen Aug 18, 2026 · Last updated Aug 19, 2026 · Updated 1 time
Summary
This study aims to build a large, multi-center database of people with IgA nephropathy, a kidney disease. Researchers will collect detailed medical information from about 2,000 participants to track how the disease progresses over time. The goal is to create a standardized resource that can support future research and improve understanding of the condition.
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
- This could lead to better ways to predict and monitor kidney disease progression in IgA nephropathy, potentially improving care and treatment decisions.
- What could go wrong
- As an observational database study, it cannot test new treatments. Its value depends on data quality and long-term follow-up, which may be incomplete.
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 2,000 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Dec 2020
- Expected to finish
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Dec 2027
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
Biopsy-proven primary IgAN patients
- Ages
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Children (under 18), adults (18 to 64) and older adults (65 and over)
- 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: 1. No age limit, no gender limit; 2. Kidney biopsy confirmed primary IgA nephropathy; 3. Sign the informed consent form voluntarily Exclusion Criteria: 1. IgA nephropathy is secondary to systemic diseases such as systemic lupus erythematosus and allergic purpura; 2. IgAN is clinically diagnosed but not confirmed by pathology; 3. The patient refuses to participate; 4. Patients judged by other investigators to be unsuitable for inclusion in the study.
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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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Ruijin Hospital, Shanghai JiaoTong University School of Medicine
RECRUITINGShanghai, Shanghai Municipality, 200025, China
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Can a transplant drug tame stubborn kidney disease?
- Blood marker may foretell kidney disease severity
- Can a new injection slow kidney disease in children?
- Mapping the Real-World treatment landscape for IgA nephropathy
- A simple test could forecast kidney disease progression
- Experimental drug aims to protect kidneys in inflammatory diseases