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Home-Based Fluid Status Monitoring in Heart Failure Patients

Home-Based Fluid Status Monitoring in Heart Failure Patients Recently Hospitalized for Acute Heart Failure

Status
Terminated
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04013373
Enrollment
92
Registered
2019-07-09
Start date
2018-10-09
Completion date
2021-07-30
Last updated
2021-08-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Heart Failure

Brief summary

This is a prospective, multi-center, single-arm study enrolling adult patients who have been hospitalized for heart failure and subsequently discharged. For the duration of study participation, patients will obtain daily at-home bioimpedance measurements. Heart failure symptoms, medications, and re-hospitalizations will be tracked. Additionally, quality of life questionnaires will be administered at the beginning and end of study participation.

Interventions

DEVICESOZO Bioimpedance Spectroscopy Device

Bioimpedance spectroscopy measurements for assessment of fluid status

Sponsors

ImpediMed Limited
Lead SponsorINDUSTRY

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
21 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Age 21 years or older 2. NYHA Class II or III at the time of study enrollment 3. Undergoing discharge following hospitalization for acute heart failure 4. Planned continued treatment for heart failure 5. Patient is able to stand or sit upright for bioimpedance spectroscopy measurements 6. Patient reports access to reliable Wi-Fi connection at home 7. Patient reports adequate space for the SOZO device at home 8. Patient provides written informed consent and authorization to use and disclose health information, including willingness to comply with study procedures

Exclusion criteria

1. Patient has an implanted cardiac rhythm management device (pacemaker or implantable cardioverter defibrillator) 2. Patient has a confirmed diagnosis of acute coronary syndrome during current admission 3. Patient is enrolled in a concurrent interventional study of an experimental treatment that may confound the results of this study, in the investigator's opinion 4. Patient has a clinical condition that would not allow them to complete the study 5. Patient has had surgical revascularization using saphenous vein grafting that may affect venous return 6. Patient is pregnant or lactating 7. Patient has nephrotic syndrome or nephrosis 8. Patient has end-stage renal disease requiring chronic dialysis 9. Patient has been diagnosed with lymphedema 10. Patient has chronic liver failure or cirrhosis 11. Patient has been diagnosed with thrombophlebitis or deep vein thrombosis in arms or legs in the past 90 days 12. Patient has an amputation of a limb \[Exception: amputation of digits may not affect bioimpedance spectroscopy measurements and will be permitted at the discretion of the study sponsor\] 13. Patient has any other medical condition that, in the opinion of the investigator, will impair the subject's ability to complete study procedures or participate in the protocol

Design outcomes

Primary

MeasureTime frameDescription
Serial bioimpedance spectroscopy (BIS) measurements including extracellular fluid and total body water45 daysCharacterize BIS trends that precede hospital readmissions for heart failure

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 15, 2026