Skip to content

urinary exosomal microRNA marker for progressive diabetic nephropathy

Product to predict the progression of diabetic nephropathy using urinary exosomal microRNA

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
CRIS
Registry ID
KCT0003573
Enrollment
270
Registered
2019-02-28
Start date
2016-10-28
Completion date
Unknown
Last updated
2019-03-25

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

Conditions

None listed

Interventions

None listed

Sponsors

Gachon University Gil Medical Center
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Type 2 diabetic patients diagnosed at the age of 30 or older - Aged 75 and younger - Patients with eGFR and albuminuria recordings at least three times in intervals of at least 3 months - Patients taking antihypertensive agents and angiotensin converting enzyme (ACE) inhibitor / angiotensin II receptor blocker (ARB) for hypertension or albuminuria have been receiving stable doses for more than 2 weeks As a healthy healthy control group, adult subjects who aged more than 30 and 75 or less years old, with neither diabetes nor chronic kidney disease

Exclusion criteria

Exclusion criteria: ? Under the age of 30 or over 75 years old ? Patients with type 1 diabetes or diabetic ketoacidosis ? Patients with CKD unrelated to diabetes ? Patients with poor blood pressure control or those taking 4 or more classes of antihypertensive drugs ? Patients with kidney transplantation or single kidney, patients with genetic kidney disease ? Among retrospective trajectory data, initial urine albumin/creation ratio (UACR)> 3500 mg/g, hemoglobin <11 g/dL, or serum albumin <3.6 g/dL ? Hemoglobin A1c level> 11.0% at enrollment, ? A history of dialysis or a history of acute kidney injury ? Other severe systemic disease or BMI <18.5 kg /square meters ? Pregnant women ? Malignant diseases with the last 5 years ? Long-term use (3 or more months) of nephrotoxic agents (e.g., NSAID and lithium) ? The use of Steroids(for 3 or more weeks) or systemic immunosuppressant dosage ? Patients who are considered inappropriate due to other clinical studies (eg, severe systemic disease, mental illness, social anxiety, etc.) ? End-stage renal disease before enrollment

Design outcomes

Primary

MeasureTime frame
MicroRNA profiles associated with the progression of diabetic nephropathy

Secondary

MeasureTime frame
Predictive performance of the combination of selected microRNA markers and clinical variables for progressive diabetic nephropathy

Countries

Korea, Republic of

Contacts

Public ContactDAE HO LEE

Gachon University Gil Medical Center

drhormone@naver.com+82-32-458-2733

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 6, 2026