Rivet PVS Therapy in Group 2 PH-HFpEF Canada

Not Applicable

Withdrawn

• Conditions: Pulmonary Hypertension; Heart Failure
• Interventions: Device: Rivet Shunt

• Registration Number: NCT05332873
• Lead Sponsor: NXT Biomedical

Brief Summary

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.

Detailed Description

Not available

Study Timeline

• Study First Submitted: 2022-04-11
• Study First Submitted QC: 2022-04-11
• Study First Posted: 2022-04-18
• Study Start: 2023-10
• Status Verified: 2024-05
• Primary Completion: 2024-05
• Last Update Submitted: 2024-05-30
• Last Update Posted: 2024-06-03
• Study Completion: 2025-05

Recruitment & Eligibility

• Status: WITHDRAWN
• Sex: All
• Target Recruitment: Not specified

Inclusion Criteria

• Age ≥ 18 years

• Prior diagnosis of Group 2 PH due to HFpEF, with at least one of the following resting hemodynamic criteria confirmed in the past year by right heart catheterization

  1. mPAP > 20 mmHg at rest
  2. mPAP/CO slope > 3 mmHg/L/min with exercise

• Confirmation of the following hemodynamic criteria during supine exercise: PCWP ≥ 25 mmHg, or PCWP/CO slope > 2 mmHg/L/min

• Chronic symptomatic heart failure documented by the following:

  1. NYHA HF Class II with history > II, or Class III, or ambulatory Class IV
  2. ≥ 1 HF hospitalization, or healthcare facility with IV diuretics or intensification of oral diuresis for HF within 12 months, or NT-pro BNP value > 400 pg/mL in normal sinus rhythm or > 750 pg/mL in atrial fibrillation in past 6 months

• Ongoing stable guideline directed medical therapy (GDMT) for HF and medically optimized per treating cardiologist according to current ACCF/AHA guidelines that is expected to be maintained without change for 1 month (excluding diuretic dosage changes for HF optimization within 30 days of the Index Procedure)

• 6MWD ≥ 100 m

Select

Exclusion Criteria

• Any therapeutic intracardiac intervention within the last 30 days

• PH Group 1, 3, 4 or 5

• Mean RAP >16 mmHg by RHC at rest on room air

• Right ventricular dysfunction, defined as one or more of the following

  1. Greater than moderate RV dysfunction as assessed by TTE and/or MRI
  2. RV FAC < 35%
  3. TAPSE < 14 mm via TTE
  4. RV size severely enlarged compared to LV size as estimated by TTE and/or MRI

• 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

• Left ventricular ejection fraction < 50%

• Severe heart failure, defined as one or more of the following:

  1. ACC/AHA/ESC Stage D heart failure, non-ambulatory NYHA Class IV HF
  2. If BMI < 30, Cardiac Index < 2.0 L/min/m2
  3. If BMI ≥ 30, Cardiac Index < 1.8 L/min/m2
  4. Requires continuous intravenous inotropic infusion
  5. Requires mechanical circulatory support
  6. Currently on the cardiac transplant waiting list

• Chronic renal dysfunction defined as: eGFR < 35 mL/min/1.73 m2 by the CKD-Epi equation

• Chronic pulmonary disease defined as one or more of the following:

  1. Requires continuous home oxygen therapy
  2. Recent hospitalization for exacerbation within 12 months prior to screening
  3. FEV1 < 50% predicted

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
Rivet Shunt Therapy	Rivet Shunt	-

Primary Outcome Measures

Name	Time	Method
Rate of Major Adverse Events	1 month	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)
Rate of Technical Success of the Rivet Shunt Implantation Procedure	At time of 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.

Secondary Outcome Measures

Name	Time	Method
Change in RV Chamber Size at 12 months - Diameter	12 months	Change in RV Chamber Size (Diameter) assessed by a core lab between baseline and 12 months
Change in Hemodynamics at 12 months - PCWP	12 Months	Change in exercise pulmonary capillary wedge pressure (PCWP) from baseline
Change in Kansas City Cardiomyopathy Questionnaire	12 months	Change in KCCQ score between baseline and 12 months.
Adverse Events through 12 months	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

Trial Locations

Locations (1)

University of Ottawa Heart Institute; 🇨🇦 Ottawa, Ontario, Canada