New registry aims to uncover real-world diabetic kidney disease care in underserved groups
NCT ID NCT07348718
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This observational study follows 2000 adults with type 2 diabetes and diabetic kidney disease from underserved communities. Researchers collect health data from medical records and questionnaires over 24 months to understand how the disease progresses and what treatments are used in routine care. No new treatments are given; the goal is to gather information to guide future studies and improve outcomes.
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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 2025
- Expected to finish
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Apr 2026
An estimate. End dates often move.
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Adults (≥18 years) with type 2 diabetes and chronic kidney disease consistent with diabetic kidney disease (e.g., reduced eGFR and/or elevated UACR) receiving routine clinical care at participating sites. Sites will primarily include safety-net systems, community hospitals, and FQHC-affiliated networks, with intentional enrollment strategies to ensure meaningful representation of underserved populations disproportionately affected by DKD. Longitudinal clinical data will be obtained from medical records, supplemented by participant questionnaires capturing patient-reported outcomes and social determinants of health.
- Ages
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18 to 70 years
- 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: Age ≥18 years at the time of enrollment Documented diagnosis of type 2 diabetes mellitus in the medical record Evidence of chronic kidney disease consistent with diabetic kidney disease (DKD), defined by one or more of the following, with evidence of chronicity (present for ≥3 months based on prior laboratory results, diagnosis codes, or clinician documentation): eGFR \<60 mL/min/1.73 m², and/or Urine albumin-to-creatinine ratio (UACR) ≥30 mg/g Receiving ongoing clinical care at a participating site with medical record data available for longitudinal follow-up Able and willing to provide written informed consent (and authorization for medical record review, as applicable) and to complete registry questionnaires Exclusion Criteria: End-stage kidney disease at baseline (maintenance dialysis) or history of kidney transplant Type 1 diabetes mellitus Known primary kidney disease not primarily attributable to diabetes that, in the investigator's judgment, is expected to drive kidney outcomes (e.g., polycystic kidney disease, active glomerulonephritis, lupus nephritis, vasculitis) Inability to provide informed consent or comply with registry procedures (e.g., no feasible longitudinal follow-up through the participating site)
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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.
Contacts and locations
Locations
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Rubix LS
Lawrence, Massachusetts, 01840, United States
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Other studies related to the condition(s) this trial covers.
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