Phase
Condition
Kidney Failure
Treatment
N/AClinical Study ID
Ages 18-40 All Genders Accepts Healthy Volunteers
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria (Patients with ADPKD):
Male and female subjects 18 - 40 years of age, inclusive
Previous diagnosis of ADPKD (based on Ravine et al. criteria)
Class 1 according to imaging classification
Estimated GFR> 70 mL/min/m2 (CKD-Epi equation)
Ability to provide written, informed consent
Inclusion Criteria (Healthy Volunteers):
Male and female subjects 18 - 40 years of age, inclusive
Estimated GFR> 90 mL/min/m2 (CKD-Epi equation)
Ability to provide written, informed consent
Exclusion Criteria (Patients with ADPKD):
Class 2 according to imaging classification
A concomitant systemic disease affecting the kidney (e.g., lupus, hepatitis B or C, amyloidosis)
Diabetes mellitus (fasting glucose > 126 mg/dL or treatment with insulin or oral hypoglycemics).
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.].
History of hypersensitivity allergic reactions to ultrasound contrast agents
High-risk cardiac disease (such as unstable hospital in-patients or ICU patients
Patients that are part of an interventional study or are taking tolvaptan
Female subjects that are pregnant
Exclusion Criteria (Healthy Volunteers):
Family and/or personal history of kidney disease
Concomitant systemic disease that may affect the kidney
Diabetes mellitus
Predicted urine protein excretion in >1 g/24 hrs, and or Abnormal urinalysis
Pregnant or lactating women
Subjects having contraindications to or interference with MRI assessments. [For example ferromagnetic metal prostheses, aneurysm clips, severe claustrophobia, large abdominal/back tattoos, etc.].
History of hypersensitivity allergic reactions to ultrasound contrast agents
High risk cardiac disease (such as unstable hospital in-patients or ICU patients
Study Design
Study Description
Connect with a study center
Mayo Clinic
Rochester, Minnesota 55905
United StatesActive - Recruiting
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