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Studies a device treatment for uncontrolled high blood pressure in older adults

Tests a kidney nerve-targeting ultrasound device in adults with uncontrolled high blood pressure.

Plain-language title generated from the registry record
Registry title: The RADIANCE CED Study

Key facts

Where
Detroit, United StatesSee the 2 sites

Where in United States

  • Henry Ford HospitalDetroit, United StatesTaking people
  • Henry Ford St. John HospitalDetroit, United StatesTaking people

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  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
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Trial details

Who runs it
ReCor Medical, Inc.
Trial code
NCT07231757
Record updated
16 July 2026
Original description
The RADIANCE CED study is a prospective observational study designed to evaluate the long-term effectiveness of ultrasound renal denervation in lowering blood pressure among patients with uncontrolled hypertension. Data will be collected from electronic health records (EHRs) of Medicare-eligible patients to support generalizability of outcomes to the broader Medicare population. Individual hospital enrollment is not required for this study and IRB exemption has been received by sponsor.Read full original descriptionShow less

The Recor Paradise System™ Hypertension Coverage With Evidence Development Study

The RADIANCE CED study is a prospective observational study designed to evaluate the long-term effectiveness of ultrasound renal denervation in lowering blood pressure among patients with uncontrolled hypertension. Data will be collected from electronic health records (EHRs) of Medicare-eligible patients to support generalizability of outcomes to the broader Medicare population. Individual hospital enrollment is not required for this study and IRB exemption has been received by sponsor.

Common Inclusion Criteria:; Adults aged ≥65 years with uncontrolled hypertension; Stable regimen of blood pressure-lowering medication; Common Exclusion Criteria:; Hypertension due to secondary causes; Prior renal denervation treatment; Pregnancy; End-stage renal disease, dialysis, or kidney transplant.

ClinicalTrials.gov NCT07231757