Real World Effectiveness of the Cordella Pulmonary Artery Sensor System in Patients With Chronic Heart Heart Failure
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Cordella PA Sensor System, Standard of Care Pharmacologic Therapy.
- Who it may be relevant to
- Registry conditions: Heart Failure NYHA Class III, Heart Failure. Basic parameters: from 18 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- United States
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Official title
The Real-World Effectiveness of The Cordella Pulmonary Artery Sensor System in Patients With Chronic Heart Failure: A Comparative Analysis to Standard of Care Pharmacologic Therapy
Overview
This retrospective, non-randomized cohort study will evaluate how well the Cordella PA Sensor System works compared to standard medication treatment in people with chronic heart failure. The study will track patients for two years to see if those using the Cordella system have fewer deaths and hospitalizations related to heart failure.
Detailed description
The study will compare two groups of patients with chronic heart failure:
* One group will use the Cordella PA Sensor System, which monitors heart pressure from home * The other group will receive standard heart failure medications without a pressure monitoring system
The main goal is to see if patients using the Cordella system have fewer heart failure-related hospital stays and a lower death rate over a two-year period. The study will look especially closely at results for:
* Men and women separately * Patients with different types of heart failure (preserved or reduced heart function) * Patients aged 75 and older * Different racial and ethnic groups * Patients with kidney disease * Patients with existing heart devices
The study will use real-world data from:
* Patients using the Cordella system in routine medical care * Similar patients receiving standard care, identified through medical records and insurance claims Both groups of patients will be carefully matched to ensure they are similar in age, gender, and other important factors that could affect the results.
Interventions
- Device Cordella PA Sensor System
* Patients who receive the Cordella PA Sensor System for monitoring chronic heart failure * These patients will be monitored for 2 years after receiving the device * Patients must be on guideline-directed medical therapy appropriate for their ejection fraction status - Drug Standard of Care Pharmacologic Therapy
* Patients with chronic heart failure who receive standard medical care without PA pressure monitoring * These patients will be monitored for 2 years * Patients must be on guideline-directed medical therapy appropriate for their ejection fraction status
Primary outcome measures
- Composite of All-cause Mortality and Heart Failure Hospitalizations [Time frame: up to 24 months]
Secondary outcome measures (5)
- Composite Outcome in Racial and Ethnic Subgroups [Time frame: up to 24 months]
- Composite Outcome in Patients with Chronic Kidney Disease [Time frame: up to 24 months]
- Composite Outcome in Patients with Cardiac Devices [Time frame: up to 24 months]
- Composite Outcome in Patients by Ejection Fraction [Time frame: up to 24 months]
- Composite Outcome in Patients Age 75+ [Time frame: up to 24 months]
Eligibility criteria
Inclusion Criteria for Cordella PA Sensor System Cohort:
- Received Cordella PA Sensor System implant between 10/1/2024-12/31/2029
- Documented chronic heart failure with NYHA Class III symptoms
- On guideline-directed medical therapy based on ejection fraction status:
- For reduced EF (≤40%): At least one fill of ACE/ARB/ARNI, MRA, BB, or SGLT2i, and one fill of a loop diuretic
- For preserved EF (>40%): At least one fill of a loop diuretic
- Has continuous health insurance enrollment for 12 months prior to implant
Inclusion Criteria for Standard of Care Control Cohort:
- Two or more encounters with diagnosis codes for chronic systolic and/or diastolic heart failure
- Documented ejection fraction reading within 6 months (+ or -) of second heart failure encounter
- On guideline-directed medical therapy based on ejection fraction status:
- For reduced EF (≤40%): At least one fill of ACE/ARB/ARNI, MRA, BB, or SGLT2i, and one fill of a loop diuretic
- For preserved EF (>40%): At least one fill of a loop diuretic
- Has continuous health insurance enrollment for 12 months prior to study entry
Exclusion criteria
- No implanted pulmonary artery sensor or monitoring at any time (Standard of Care Control Cohort only)
- Record of temporary mechanical circulatory support during baseline period
- Diagnosis of cardiogenic shock during baseline period
- Receiving palliative care/hospice during baseline period
- Record of end-stage renal disease during baseline period
- Unable to take dual antiplatelet therapy or anticoagulants for one month post implant (Cordella Cohort only)
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Observational model
- Cohort
Study locations
United States · 1 center
- Endotronix — Naperville
Identifiers
NCT: NCT06783335 · OS-2025-001