N/A
N=46
PRospective Evaluation of Electrocardiographic Voltage Changes and Six Minute Walk Test for Predicting Readmissions in Heart Failure (PREEMT-HF Study)
Heart Failure
Bottom Line
View on ClinicalTrials.gov: NCT01675544 ↗Enrolled (actual)
46
Serious AEs
0.0%
Results posted
Sep 2014
Primary outcome: Primary: Emergency Room Visit or Hospitalization for Acute Decompensated Heart Failure (ADHF) — 20 participants
Study Design & Population
- Study type
- Observational
- Phase
- N/A
- Interventions
- Electrocardiogram (Procedure); Six minute walk test (Procedure)
- Age
- Adult, Older Adult · 19+ yrs
- Sex
- All
- Sponsor
- Creighton University
- Primary completion
- Jun 2014
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Emergency Room Visit or Hospitalization for Acute Decompensated Heart Failure (ADHF) |
20 | — |
| PRIMARY Mortality |
9 | — |
Summary
Purpose of the study: To identify whether Electrocardiographic QRS voltage changes (between admission and pre-discharge) and pre discharge 6- minute walk test in patients admitted with acute heart failure can identify patients at risk for recurrent admissions for heart failure.
Eligibility Criteria
Inclusion Criteria
- Patients > 18 years of age, admitted with a diagnosis of ADHF and fulfilling the following criteria:
- Evidence of systemic congestion (manifested by any 2 of the following criteria: jugular venous distension, edema, pulmonary rales, Left ventricular S3, or radiographic evidence of pulmonary venous congestion)
- Elevated Brain natriuretic peptide
- Need for at least 1 dose of intravenous loop diuretic
Exclusion Criteria
- Cardiogenic shock, Acute coronary syndromes (patients with mild elevation in troponin related to heart failure will not be excluded), patients who are admitted for another principal problem and develop ADHF in the hospital, pregnant females, end stage renal disease on hemodialysis, expected survival < 6 months.
Data sourced from ClinicalTrials.gov (NCT01675544). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.