Can a blood pressure procedure spare the kidneys?
NCT ID NCT07786636
First seen Aug 26, 2026 · Last updated Aug 27, 2026 · Updated 1 time
Summary
This study looks at how renal denervation, a minimally invasive procedure for hard-to-treat high blood pressure, affects kidney function shortly after and up to a year later. Researchers will measure kidney function and analyze blood and urine samples from 50 adults with resistant hypertension. The goal is to see if the procedure causes changes in the kidneys and whether those changes relate to better kidney health over time.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Renal denervation procedure
- What this could lead to
- If successful, this could clarify how renal denervation impacts kidney health, potentially guiding better use of the procedure for resistant hypertension.
- What could go wrong
- This is an observational study with a small sample size, so findings may not apply broadly. The procedure itself carries risks, and the study does not test a new treatment.
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.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 50 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Sep 2026
An estimate. Start dates often move.
- Expected to finish
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Aug 2028
An estimate. End dates often move.
- Lead sponsor
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A research network
The lead sponsor is a research network or cooperative group.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- 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: * ≥18 years * eGFR \>30 ml/min/1.73m2 (CKD stages 3b and less severe) * Informed consent for study participation provided by the patient or the legal guardian * Patient information and consent to the processing of personal data * Stable therapy in the previous three months * All patients undergoing RDN for clinical indications Exclusion Criteria: * Patients in emergency situations * Turbid urine sample on admission * Visible haematuria in the urine sample on admission * Pregnancy * Allergy to contrast media (visipaque, omnipaque, iohexol) * Any problem, which, in the investigator's opinion, might jeopardize the participant's compliance with the protocol.
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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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
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