Gas Exchange for Predicting Hospital Heart Failure Readmissions
Status: | Completed |
---|---|
Conditions: | Cardiology |
Therapuetic Areas: | Cardiology / Vascular Diseases |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 4/2/2016 |
Start Date: | October 2013 |
End Date: | January 2015 |
Gas Exchange for Predicting Hospital Heart Failure Readmissions Clinical Evaluation Study
To determine whether, and if so, which gas exchange parameters measured on the Shape-HF
Cardiopulmonary Exercise Testing System predict 30 and 180 day re-hospitalization in
subjects discharged from hospitalization for an episode of acute decompensated heart
failure.
Cardiopulmonary Exercise Testing System predict 30 and 180 day re-hospitalization in
subjects discharged from hospitalization for an episode of acute decompensated heart
failure.
This is a prospective, single-specialty clinical study. This study is intended to evaluate
the select gas exchange parameters during a short, sub-max bout of exercise using a simple
stationary step on day of discharge to predict the subjects' readmission for acute
decompensated heart failure.
the select gas exchange parameters during a short, sub-max bout of exercise using a simple
stationary step on day of discharge to predict the subjects' readmission for acute
decompensated heart failure.
Inclusion Criteria:
- Subject is 18 Years and older
- Subject is hospitalized for acute decompensated heart failure (ADHF)
1. Systolic OR
2. Diastolic
- Subject is Stage C:Class II/III/IV heart failure
- Subject is willing and to provide appropriate informed consent
- Subject is willing and able to comply with the requirements of the protocol,
including follow-up evaluations and schedule
- Subject is willing to use the Shape-HF Cardiopulmonary Exercise Testing System
Exclusion Criteria:
- The subject is pregnant (verified in a manner consistent with institution's standard
of care)
- Subject is currently participating in another investigational device or drug trial
- Subject is a prisoner, a minor or unable to adequately give informed consent due to
mental or physical condition
- Subject is unwilling or unable to return for the required follow-up after test
- Subject has Left Ventricular Assist Device (LVAD)
- Subject is listed for transplant
- Subject has a clinical diagnosis of acute myocardial infarction (AMI) on admission
(Note: If troponin measurements have been collected and are elevated but not due to
an MI subject is still eligible for study)
- Subject has a pulmonary embolism (PE) on admission
- Subject is dialysis dependent
- Subject has a cardiac resynchronization device (CRT) which has been re-programmed at
any time during the study
- Subject has Chronic Obstructive Pulmonary Disease (COPD) who is oxygen or steroid
dependent
- Subject has severe hypertension > 180 millimeter of mercury (mmHg) resting systolic
at time of test
- Subject has severe heart failure with renal insufficiency (with Creatinine clearance
rate (CrCL) of 30 or less) and/or on IV Inotropic therapy and/or enrolling in hospice
We found this trial at
7
sites
Cleveland Clinic Cleveland Clinic is committed to principles as presented in the United Nations Global...
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Univ of Minnesota With a flagship campus in the heart of the Twin Cities, and...
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