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New ultrasound technique could spot kidney damage earlier in ADPKD

NCT ID NCT05288998

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing This study
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study is testing a new type of ultrasound called super-resolution ultrasound (SRU) to get a detailed look at the tiny blood vessels in the kidneys. Researchers will compare images from 34 people with ADPKD and healthy volunteers to see if SRU can detect differences in blood flow and vessel structure. The goal is to develop a noninvasive way to monitor kidney health in ADPKD without needing a biopsy or contrast dye.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

What this could lead to
If successful, this imaging method could help doctors monitor kidney damage in ADPKD without invasive procedures, potentially leading to earlier detection of disease progression.
What could go wrong
This is a small, early-stage study focused on testing a new imaging technique, not a treatment. The method may not prove reliable or useful in larger, more diverse groups.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Participants

34 people

The number who actually took part.

Started

Nov 2021

Expected to finish

Dec 2026

An estimate. End dates often move.

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Who is studied

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

Ages

18 to 40 years

Sex

Anyone

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

Show 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 (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

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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

  • Mayo Clinic

    Rochester, Minnesota, 55905, United States

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