Hospital Admission in Heart Failure: Readiness for Discharge and Predicting Future Admissions
Overview
Tab Title Description
Study type
ObservationalDescribes the nature of a clinical study. Types include:
- Observational study — observes people and measures outcomes without affecting results.
- Interventional study (clinical trial) — studies new tests, treatments, drugs, surgical procedures or devices.
- Medical records research — uses historical information collected from medical records of large groups of people to study how diseases progress and which treatments and surgeries work best.
Study IDs
Site IRB
- Rochester, Minnesota: 11-002371
Sponsor Protocol Number: 11-002371
About this study
The purpose of this study is to identify measures of heart rate and heart rate variability responses to changes in nervous system activity, breathing variability, and lung fluid in HF patients as early as possible in the course of their hospital admission and subsequently just prior to discharge, using a simplified approach, in order to determine if these measures can assess readiness for discharge and more accurately predict likelihood for readmission.
Participation eligibility
Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Contact the study team to discuss study eligibility and potential participation.
Inclusion Criteria:
- Patients with New York Heart Association (NYHA) class I-IV HF, regardless of left ventricular functional status.
- These patients will be on stable doses of optimized medications (including β-blockers, angiotensin-converting enzyme inhibitors or angiotensin receptor blockers, and diuretics) for at least 1 month prior to enrollment.
- Subjects with allergies or skin sensitivities to electrode hydrogel and/or acrylic based adhesive, subjects with skin breakdown in areas on the chest where device placement is required or subjects with Neurostimulators will also not be able have thoracic fluid status accessed using the µ-cor device, but could complete all other parts of the study.
- The majority of patients will be recruited from the Heart Failure Clinic and the Cardiovascular Health Clinic (CVHC) in the Division of Cardiovascular Diseases of Mayo Clinic, as well as from the surrounding community.
Exclusion Criteria:
- Subjects recruited must not be pregnant or trying to become pregnant (this will be confirmed with a blood pregnancy test at the SMH CRU before any testing begins).
Participating Mayo Clinic locations
Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.
| Mayo Clinic Location |
Status |
|
Rochester, Minn.
Mayo Clinic principal investigator Bruce Johnson, Ph.D. |
Closed for enrollment |
|
More information
Publications
Publications are currently not available