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The RADIANCE CED Study
NCT07231757 · View on ClinicalTrials.gov ↗
Study Summary
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.
Conditions Studied
Interventions
- DEVICE Ultrasound Renal Denervation (Paradise™ Ultrasound Renal Denervation (uRDN) System)
Study Locations (1)
Michigan
- Henry Ford St. John Hospital — Detroit
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 1,000 participants |
| Start Date | 2025-11-21 |
| Est. Completion | 2031-12-31 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT07231757
The ClinicalTrials.gov registry entry for NCT07231757 describes a study currently listed as recruiting. It is categorized as an unspecified phase, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 1,000 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is ReCor Medical, which has 5 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 3 conditions, with Hypertension appearing as the primary indexed condition, and to 1 intervention — of which Ultrasound Renal Denervation (Paradise™ Ultrasound Renal Denervation (uRDN) System) is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT07231757 reports 1 study location spanning 1 distinct geographic area — top geographies include Michigan. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT07231757 about?
NCT07231757 is a clinical study titled "The RADIANCE CED 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 pat...
What is the current status of trial NCT07231757?
This trial is currently recruiting. The enrollment target is 1,000 participants. The study started on 2025-11-21. Estimated completion is 2031-12-31.
What conditions does trial NCT07231757 study?
This clinical trial studies the following conditions: Hypertension, Cardiovascular Diseases, Vascular Diseases. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT07231757?
The interventions under investigation include: Ultrasound Renal Denervation (Paradise™ Ultrasound Renal Denervation (uRDN) System) (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT07231757?
This trial is sponsored by ReCor Medical, which has 5 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT07231757 being conducted?
This trial has 1 study location across Michigan. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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