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Commercial decision
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This clinical investigation is a prospective, multicenter, non-randomized, open-label, Early Feasibility Study to evaluate the safety, performance, and initial clinical efficacy of the Rivet PVS therapy in patients with symptomatic pulmonary hypertension.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Rivet Shunt Therapy | Experimental |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Rivet Shunt | Device | The Rivet Shunt device will be implanted via a percutaneous, transcatheter approach |
|
| Measure | Description | Time Frame |
|---|---|---|
| Rate of Major Adverse Events | Composite of major adverse cardiac, cerebrovascular, or renal events (MACCRE) and re-intervention for study device related complications at implantation procedure (Day 0) and up to 1-month post-procedure (Day 30) | 1 month |
| Rate of Technical Success of the Rivet Shunt Implantation Procedure | Study device is implanted as intended and confirmation of a patent pulmonary-to-venous shunt between the RPA and SVC by qualitative assessment via angiography and/or echocardiography at implantation procedure. | At time of procedure |
| Measure | Description | Time Frame |
|---|---|---|
| Adverse Events through 12 months | Composite of MACCRE and re-intervention for study device related complications (as described above), progression of PH and/or HF disease, and all-cause mortality to 12 months post-procedure | 12 months |
| Change in Hemodynamics at 12 months - PCWP |
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Select Inclusion Criteria:
Age ≥ 18 years
Prior diagnosis of Group 2 PH due to HFpEF, with the following resting hemodynamic criteria confirmed in the past year by right heart catheterization
a. mPAP ≥ 25 mmHg at rest or mPAP/CO slope > 3 mmHg/L/min during incremental exercise
Confirmation of the following hemodynamic criteria during supine exercise
a. PCWP ≥ 25 mmHg, or PCWP/CO slope > 2 mmHg/L/min
Chronic symptomatic heart failure documented by the following:
Ongoing stable guideline directed medical therapy (GDMT) for HF and medically optimized per treating HF physician according to current ACCF/AHA guidelines that is expected to be maintained without change for 6 months (excluding diuretic dosage changes for HF optimization within 90 days of the Index Procedure)
6MWD ≥ 150 m
Select Exclusion Criteria:
Any therapeutic intracardiac intervention within the last 30 days
PH Group 1, 3, 4 or 5
Mean RAP >12 mmHg by RHC at rest on room air
Right ventricular dysfunction, defined as one or more of the following
Severe tricuspid valve regurgitation
Peak systolic pulmonary arterial pressure > 80 mmHg by RHC at rest while awake
Mean pulmonary arterial pressure > 50 mmHg by RHC at rest while awake
PVR > 6 Wood units at rest while awake on room air or exercise PVR > 2 Wood Units
Left ventricular ejection fraction < 50%
Severe heart failure, defined as one or more of the following:
Chronic renal dysfunction defined as one or more of the following:
Chronic pulmonary disease defined as one or more of the following:
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Massachusetts General Hospital | Boston | Massachusetts | 02114 | United States | ||
| Mayo Clinic |
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| ID | Term |
|---|---|
| D006333 | Heart Failure |
| D006976 | Hypertension, Pulmonary |
| ID | Term |
|---|---|
| D006331 | Heart Diseases |
| D002318 | Cardiovascular Diseases |
| D008171 | Lung Diseases |
| D012140 | Respiratory Tract Diseases |
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Change in exercise pulmonary capillary wedge pressure (PCWP) from baseline |
| 12 Months |
| Change in Kansas City Cardiomyopathy Questionnaire | Change in KCCQ score between baseline and 12 months. | 12 months |
| Change in RV Chamber Size at 12 months - Diameter | Change in RV Chamber Size (Diameter) assessed by a core lab between baseline and 12 months | 12 months |
| Change in Hemodynamics at 12 months - mPAP/CO Slope | Change in exercise mPAP/CO Slope (mean pulmonary artery pressure/cardiac output slope) from baseline | 12 months |
| Change in RV function at 12 months - RV Fractional Area Change (FAC) | Change in RV FAC assessed by a core lab between baseline and 12 months | 12 months |
| Rochester |
| Minnesota |
| 55905 |
| United States |
| UVA Cardiology Research | Charlottesville | Virginia | 22908 | United States |
| D006973 |
| Hypertension |
| D014652 | Vascular Diseases |