Condition: Hypertension · Cardiovascular Diseases · Vascular Diseases · Sponsor: ReCor Medical, Inc.
The objective of the Global Paradise® System US Post Approval Study (US GPS) is to evaluate the real-world use of the Paradise Ultrasound Renal Denervation System indicated for patients who are unable to lower their blood pressure with lifestyle changes and medication. This system is comprised of a catheter, cable, balloon, and generator and has received FDA approval in the United States. Information collected in this study will be analyzed to better understand the long-term safety and effectiveness of treatment with the Paradise System for patients with high blood pressure.
This description comes directly from the study's public registry record.
Helen Reeve-Stoffer, PhD · +1 650-912-9032 · hreeve-stoffer@recormedical.com
Liz Sheehan · Liz.Sheehan@recormedical.com
Always discuss trial participation with your own doctor first.
| Sutter Institute for Medical Research | Sacramento, California, United States | Recruiting |
| UC Davis Medical Center | Sacramento, California, United States | Recruiting |
| Pacific Heart Institute | Santa Monica, California, United States | Recruiting |
| Rocky Mountain Regional VAMC | Aurora, Colorado, United States | Recruiting |
| Bridgeport Hosptial | Bridgeport, Connecticut, United States | Recruiting |
| The Cardiac & Vascular Institute | Gainesville, Florida, United States | Recruiting |
| University of Miami Health System | Miami, Florida, United States | Recruiting |
| Ascension Sacred Heart | Pensacola, Florida, United States | Recruiting |
| Tampa Cardiovascular Interventions and Research | Tampa, Florida, United States | Recruiting |
| Wellstar Kennestone Hospital | Marietta, Georgia, United States | Recruiting |
| Southern Illinois University, Memorial Medical Center | Springfield, Illinois, United States | Recruiting |
| Ascension via Christi St. Francis | Wichita, Kansas, United States | Recruiting |
+ 27 more locations — full list on the registry record.
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Source record: clinicaltrials.gov/study/NCT06297291