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Bio-impedance monitoring in patients hospitalized with acute decompensated heart failure

Assessing the haemodynamic status, invasively and non-invasively, in patients hospitalized with acute decompensated heart failure (part II)

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON23218
Enrollment
20
Registered
2015-08-11
Start date
2015-07-10
Completion date
Unknown
Last updated
2024-02-28

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

Conditions

Heart Failure, Acute Heart Failure

Interventions

None listed

Sponsors

Philips Research Eindhoven
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: - Age ≥ 18 years - Presence of an impedance-enabled CRT and/or ICD device > 2 months - Hospitalized because of symptoms/ signs of decompensation - Objective evidence of cardiac dysfunction - NTproBNP on admission > 450 pg/ml - Follow-up exclusively in the OLV Hospital of Aalst - Need for treatment with diuretics (IV or oral), in higher dose than maintenance dose

Exclusion criteria

Exclusion criteria: - Severe pulmonary disease (one minute forced expiratory volume below 1.0L/s) - Poor echo window - Anticoagulant therapy - Need for ventilation - Prisoners - Pregnancy

Design outcomes

Primary

MeasureTime frame
The ability of the device data to detect improvements in haemodynamic status.

Secondary

MeasureTime frame
Prognostic ability of the device data at discharge and 6-month re-admission or death.

Contacts

Public ContactRiet Dierckx

OLV Hospital - Study Cardiology

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)