RecruitingPhase not listed

HF2 Registry - Hemodynamic Frontiers in Heart Failure Registry

Hemodynamic Frontiers in Heart Failure Registry

Who can join

As published by the study on ClinicalTrials.gov. "Not stated" means the study hasn't said — ask the study team.

Age
18 Years to 100 Years
Sex
All sexes
Healthy volunteers
Not accepted
Compensation
Not stated

Other requirements are listed under Eligibility below. Only the study team can confirm whether you can join.

What to expect

No one can promise a trial will help you personally — that is what the research is trying to find out.

What participation involves

Not stated in the study description — ask the study team about visits and procedures.

Compensation
Not stated
  • Study-related exams and procedures are typically provided at no cost. This is how many trials work in general — confirm the details for this study with the study team.
  • Participants are monitored closely by the research team throughout the study.
  • Some participants may receive access to an investigational treatment, which is still being studied.
  • Your participation helps researchers learn whether this approach could help future patients.

About this study

The purpose of the HF2 (Hemodynamic Frontiers in Heart Failure) registry is to collect relevant patient-level demographic, clinical, laboratory, and hemodynamic data from patients implanted with pulmonary artery pressure sensor at participating centers to advance scientific knowledge about ambulatory hemodynamics monitoring and HF (Heart Failure) therapies. The data collected will be used for retrospective studies, quality improvement, identifying research cohorts, and member-initiated research.

Compensation is read from the study's own description and may be missing — always confirm with the study team.

Eligibility

Official eligibility criteria

Inclusion Criteria: 1. All patients would have been or will be implanted per indications from FDA approval/CHAMPION trial. These would be patients with NYHA (New York Heart Association) Class III heart failure who had a prior hospitalization. 2. Patients who meet the expanded FDA indication (BNP elevation without hospitalization or NYHA class II). Exclusion Criteria: 1. Patients less than 18 years of age. 2. Pregnant women at the scheduled time of PA pressure sensor implant. 3. Patients unable or unwilling to have continuity of care in the heart failure clinic.

Study sites (12)

CA

  • Scripps Health · La Jolla, CA 92037Timothy Jordan, MD · Study contactThomas Heywood, MD · Principal investigatorMore trials in La Jolla

IN

  • Indiana University · Bloomington, IN 47401Maya Guglin, MD · Study contactMaya Guglin, MD · Principal investigatorMore trials in Bloomington

KS

MN

  • Fairview Health · Maplewood, MN 55109Terrie-Ann Benjamin, MD · Study contactTerrie-Ann Benjamin, MD · Principal investigatorMore trials in Maplewood
  • Minneapolis Heart Institute Foundation/ Allina Health · Minneapolis, MN 55407Sarah Schwager, RN · Study contactMosi Bennett, MD · Principal investigatorMore trials in Minneapolis

MO

  • Saint Luke's Health System · Kansas City, MO 64131Timothy Fendler, MD · Study contactTimothy Fendler, MD · Principal investigatorMore trials in Kansas City

NC

  • University of North Carolina/ Rex Hospital, Inc. · Raleigh, NC 27607Elizabeth Volz, MD · Study contactElizabeth Volz, MS · Principal investigatorMore trials in Raleigh

OR

  • Providence Heart Institute · Portland, OR 97225Christy Lenhart, RN · Study contactJacob Abraham, MD · Principal investigatorMore trials in Portland

SC

  • Prisma Health · Columbia, SC 29203Suzanne Amaker · Study contactPatrick McCann, MD · Principal investigatorMore trials in Columbia

SD

  • Sanford Health · Sioux Falls, SD 57104Orvaar Jonsson, MD · Study contactOrvaar Jonsson, MD · Principal investigatorMore trials in Sioux Falls

TX

  • Austin Heart · Austin, TX 78756Kunjan Bhatt, MS · Study contactKunjan Bhatt, MD · Principal investigatorMore trials in Austin
  • Houston Methodist DeBakey Heart and Vascular Center · Houston, TX 77030Saba Khan · Study contactAshrith Guha, MD · Principal investigatorArvind Bhimaraj, MD · Principal investigatorMore trials in Houston