Intrarenal Microvasculature in ADPKD

January 15, 2026 updated by: Maria V. Irazabal Mira, Mayo Clinic

Noninvasive Evaluation of the Intrarenal Microvasculature in ADPKD

The primary objective of this study is to evaluate the use of Super-resolution ultrasound (SRU) to assess the intrarenal microvasculature in patients with Autosomal Dominant Polycystic Kidney Disease (ADPKD) and healthy volunteers.

Study Overview

Status

Active, not recruiting

Detailed Description

An intact intrarenal microcirculation is vital to preserving normal kidney function, and microvascular dysfunction, damage, and loss are known to contribute to renal function decline. In ADPKD, extensive vascular remodeling has been proposed to play an important role in its progression. However, microvascular analyses in rodents and humans with ADPKD have been performed ex vivo or in vitro and from kidneys removed at the time of renal failure due to the invasive nature and additional limitations of the currently available techniques. A non-invasive and direct method to assess the intrarenal microvasculature is needed to improve early detection and gauge the progression of microvascular alterations and monitor the success of therapeutic approaches.

Current imaging modalities, such as micro-computed tomography, magnetic resonance imaging, and contrast-enhanced ultrasound, have attempted to provide a non-invasive assessment of the intrarenal microvasculature in pre-clinical models of kidney diseases. However, each of these modalities has important limitations when translating into humans, including high cost, requiring long imaging times, using nephrotoxic contrast agents, radiation exposure, low spatial resolution, and poor reproducibility.

Super-resolution ultrasound (SRU) imaging is among the most rapidly advancing imaging techniques introduced to overcome the limitation of the inherent spatial resolution of ultrasound. With the use of non-nephrotoxic contrast microbubbles to break the diffraction limit of ultrasound, and the introduction of ultrasound localization microscopy which utilizes ultrafast frame rate imaging to reconstruct a super-resolved composite image, SRU has provided a paradigm-shifting tool for structural and functional evaluation of tissue microvasculature. However, in vivo, human imaging, and kidney imaging pose significant organ depth challenges (which results in ultrasound signals with lower signal-to-noise ratio) and physiologic and operator-induced motion (which reduces the available data accumulation time). Our team recently implemented advanced filtering and microbubble localization and tracking techniques to overcome these limitations, which extract only microbubble signals and reliably pinpoint the center of each microbubble from the extracted signals.

The investigators' broad objective is to deploy and evaluate the use of SRU imaging coupled with advanced post-processing techniques to assess the intrarenal microvasculature in patients with early ADPKD and healthy volunteers.

Participants in this study will have a renal ultrasound to determine intrarenal microvascular parameters, and an abdominal MRI to determine the patient's total kidney volume (TKV), and additional vascular parameters. In addition, participants will have a blood and a urine sample collected to determine biomarkers of endothelial function and injury.

Study Type

Observational

Enrollment (Actual)

34

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Minnesota
      • Rochester, Minnesota, United States, 55905
        • Mayo Clinic

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 40 years (Adult)

Accepts Healthy Volunteers

Yes

Sampling Method

Non-Probability Sample

Study Population

Patients with a previous diagnosis of ADPKD that meet the inclusion criteria, and healthy volunteers

Description

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> 90 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 Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Patients with a previous diagnosis of ADPKD
Patients that have been diagnosed with ADPKD and meet the study's inclusion criteria
Healthy Volunteers
Subjects without a family or personal history of kidney disease or concomitant systemic disorder that might affect the kidney

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Assessment of intrarenal microvascular density in HV and patients with ADPKD
Time Frame: Baseline
Renal vessel density as percentage, determined by SRU.
Baseline
Assessment of intrarenal microvascular flow speed in HV and patients with ADPKD
Time Frame: Baseline
Microvascular flow speed (mm/s), determined by SRU.
Baseline
Assessment of intrarenal microvascular perfusion in HV and patients with ADPKD
Time Frame: Baseline
Intrarenal perfusion (mm/s), determined by SRU.
Baseline
Assessment of intrarenal tortuosity indices in HV and patients with ADPKD
Time Frame: Baseline
Tortuosity indices defined as sum of angles metric (SOAM) (rad/mm), determined by SRU
Baseline

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Inter-sonographer variability of the intrarenal microvasculature
Time Frame: Baseline
Second US at the same visit performed by a different sonographer, and used to calculate the intraclass correlation coefficient
Baseline
Day-to-day variability of intrarenal microvasculature in healthy volunteers
Time Frame: Baseline to 7 days
A second US within 1-7 days is performed by the same sonographer, to determine the within-person variability for each of the primary outcome measures
Baseline to 7 days
Patient-to-patient variability in patients with ADPKD
Time Frame: Baseline
Correlation between primary outcome measures and image class (A, B, C, D and E) as determined by the Image classification.
Baseline

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Investigators

  • Principal Investigator: Maria V Irazabal, M.D., Ph.D, Mayo Clinic

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

November 30, 2021

Primary Completion (Estimated)

December 1, 2026

Study Completion (Estimated)

December 1, 2026

Study Registration Dates

First Submitted

February 21, 2022

First Submitted That Met QC Criteria

March 11, 2022

First Posted (Actual)

March 21, 2022

Study Record Updates

Last Update Posted (Estimated)

January 16, 2026

Last Update Submitted That Met QC Criteria

January 15, 2026

Last Verified

January 1, 2026

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

Clinical Trials on Autosomal Dominant Polycystic Kidney Disease

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