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NCT04344769Recruiting

Characterization of the Nrf2 Response in Patients With Autosomal Dominant Polycystic Kidney Disease (ADPKD)

Source: ClinicalTrials.gov · Last updated 16 Jan 2026

Brief summary (registry, in English)

The purpose of this study is to characterize oxidative stress and the Nrf2 antioxidant response in early stages of Autosomal Dominant Polycystic Kidney Disease (ADPKD), while identifying candidate biomarkers.

Status (registry)
Recruiting
Study type
Observational
Enrollment
40 (estimated)
First submitted
10 Apr 2020
Start date
4 Oct 2019
Primary completion date
Dec 2026
Lead sponsor
Mayo Clinic
NCT number
NCT04344769

What you commit to

  • Study type: Observational
  • Planned participants: 40
  • From 4 Oct 2019 to the primary completion date, Dec 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Concomitant systemic disease in the kidney (e.g. lupus, hepatitis B or C, amyloidosis)
  • Abnormal urinalysis suggestive of concomitant glomerular disease.
  • Previous personal or family history of kidney disease.
  • Concomitant systemic disease in the kidney (e.g. lupus, hepatitis B or C, amyloidosis)

Other illness

  • Abnormal urinalysis suggestive glomerular disease.

Lab values

  • Diabetes mellitus (fasting glucose \> 126 mg/dL or treatment with insulin or oral hypoglycemics).
  • Diabetes mellitus (fasting glucose \> 126 mg/dL or treatment with insulin or oral hypoglycemics).

Other

  • Class 2 according to our imaging classification
  • Predicted urine protein excretion in urinalysis \>1 g/24 hrs
  • Subjects having contraindications to, or interference with MRI assessments. \[For example: ferromagnetic metal prostheses, aneurysm clips, severe claustrophobia, large abdominal/back tattoos, etc\].
  • Female subjects that are pregnant
  • Presence of proteinuria
  • Subjects having contraindications to, or interference with MRI assessments. \[For example: ferromagnetic metal prostheses, aneurysm clips, severe claustrophobia, large abdominal/back tattoos, etc\]
  • Female subjects that are pregnant

Who the study is looking for

  • ADPKD (based on Ravine et al. criteria)
  • Class 1 B-E according to our imaging classification
  • Male and female subjects 18 - 30 years of age, inclusive
  • Estimated GFR\> 60 mL/min/m2 (CKD-EPI equation)
  • Ability to provide written, informed consent.
  • Male and female subjects 18 - 30 years of age, inclusive
  • Estimated GFR\> 60 mL/min/m2 (CKD-EPI equation)
  • Ability to provide written, informed consent.

Age in the registry: 18 years to 30 years · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Mayo Clinic in Rochester
Coordinator of this site? Confirm its status
RochesterUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.