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NCT06052072 · ClinicalTrials.gov registry record · NA
Pulmonary Artery DenerVation Clinical Study Using the Gradient Denervation System in Heart Failure Patients With Pulmonary Hypertension Group 2 (PreVail-PH2 Study)
A NA study of Heart Failure and Group 2 Pulmonary Hypertension, sponsored by Gradient Denervation Technologies.
- Recruiting
- Registry status
- NA
- Development phase
- 50
- Enrollment target
- 8
- Study locations
NCT06052072 is a NA study of Heart Failure and Group 2 Pulmonary Hypertension that is actively recruiting participants, run by Gradient Denervation Technologies. The registered enrollment target is 50 participants, below the 2,049-participant average among 397 other Heart Failure trials with a reported enrollment target (98% lower). The trial reports 8 study locations across 6 states.
The verdict
NCT06052072, a NA study of Heart Failure and Group 2 Pulmonary Hypertension, is actively recruiting participants, sponsored by Gradient Denervation Technologies.
- RECRUITING
- Registry status
- NA
- Development phase
- 50 participants
- Enrollment target
- 8
- Study locations
Study Summary
This early feasibility study is intended to characterize the impact of pulmonary artery denervation on the quality of life in Heart Failure Patients with Group 2 Pulmonary Hypertension
Conditions Studied
Interventions
- DEVICE Gradient Denervation System
Study Locations (8)
Texas
- Baylor College of Medicine - Houston
- Houston Methodist - Houston
Wisconsin
- University of Wisconsin - Madison
- Aurora Health - Milwaukee
Illinois
- Northwestern University - Chicago
Massachusetts
- Massachusetts General Hospital - Boston
North Carolina
- Duke University - Durham
South Carolina
- Medical University of South Carolina - Charleston
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 50 participants |
| Start Date | 2024-02-20 |
| Est. Completion | 2028-07-01 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06052072
The ClinicalTrials.gov registry entry for NCT06052072 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 50 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 2,049-participant average among 397 other Heart Failure trials with a reported enrollment target (98% lower). The listed sponsor is Gradient Denervation Technologies, which has 1 total studies on file at ClinicalTrials.gov.
The record links to 2 conditions, with Heart Failure appearing as the primary indexed condition, and to 1 intervention - of which Gradient Denervation System is the first listed.
NCT06052072 reports 8 study locations spanning 6 distinct geographic areas - top geographies include Texas, Wisconsin, Illinois.
Frequently Asked Questions
What is clinical trial NCT06052072 about?
NCT06052072 is a clinical study titled "Pulmonary Artery DenerVation Clinical Study Using the Gradient Denervation System in Heart Failure Patients With Pulmonary Hypertension Group 2 (PreVail-PH2 Study)". This early feasibility study is intended to characterize the impact of pulmonary artery denervation on the quality of life in Heart Failure Patients with Group 2 Pulmonary Hypertension
What is the current status of trial NCT06052072?
This trial is currently recruiting. It is a NA study. The enrollment target is 50 participants. The study started on 2024-02-20. Estimated completion is 2028-07-01.
What conditions does trial NCT06052072 study?
This clinical trial studies the following conditions: Heart Failure, Group 2 Pulmonary Hypertension.
What interventions are being tested in trial NCT06052072?
The interventions under investigation include: Gradient Denervation System (DEVICE).
Who is sponsoring clinical trial NCT06052072?
This trial is sponsored by Gradient Denervation Technologies, which has 1 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06052072 being conducted?
This trial has 8 study locations across Illinois, Massachusetts, North Carolina, South Carolina, Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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