New study links blood markers to kidney disease progression in ADPKD
NCT ID NCT05193981
First seen Jun 27, 2026 ยท Last updated Jun 27, 2026
Summary
This study looks at how certain blood chemicals and blood vessel function relate to kidney disease severity in people with early-stage Autosomal Dominant Polycystic Kidney Disease (ADPKD). Researchers will measure homocysteine levels and blood vessel health in 80 participants aged 15-40. The goal is to find markers that can predict how fast the disease progresses, which may help guide future treatments.
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Study facts
What this study's own registry entry says, in plain language.
- Participants
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80 people
The number who actually took part.
- Started
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Sep 2021
- Expected to finish
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Dec 2026
An estimate. End dates often move.
- Lead sponsor
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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
Male and female patients with a previous diagnosis of ADPKD that meet the inclusion criteria.
- Ages
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15 to 40 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide 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: * Male and Female subjects, 15-40 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/1.73m\^2(CKD-EPI) * Ability to provide written, informed consent. Exclusion Criteria: * Class 2 according to imaging classification * A concomitant systemic disease affecting the kidney * Diabetes mellitus * Predicted urine protein excretion in urinalysis \>1 g/24 hrs * Subjects having contraindications to or interference with MRI assessments * Patients that are part of an interventional study or taking tolvaptan * Female subjects that are pregnant
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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
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Mayo Clinic
Rochester, Minnesota, 55905, United States
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Other studies related to the condition(s) this trial covers.
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