No registrations found.
ID
Source
Health condition
Heart Failure, Acute Heart Failure
Sponsors and support
Intervention
Outcome measures
Primary outcome
The ability of the device data to detect improvements in haemodynamic status.
Secondary outcome
Prognostic ability of the device data at discharge and 6-month re-admission or death.
Study objective
The primary objective of this study is to explore the correlation between invasive and non-invasive haemodynamic variables and monitor the effect of treatment during admission for acute decompensated heart failure. In particular to investigate correlations between device data (trans-thoracic impedance) and invasive measures of pulmonary capillary wedge pressures.
The secondary objective is to investigate the relationship between device data at discharge and risk of readmission/death at 6 months.
Intervention
N/A
Riet
Dierckx
Moorselbaan 164
9300
Riet
Dierckx
Moorselbaan 164
9300
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
- Severe pulmonary disease (one minute forced expiratory volume below 1.0L/s)
- Poor echo window
- Anticoagulant therapy
- Need for ventilation
- Prisoners
- Pregnancy
Design
Recruitment
Followed up by the following (possibly more current) registration
No registrations found.
Other (possibly less up-to-date) registrations in this register
No registrations found.
In other registers
| Register | ID |
|---|---|
| NTR-new | NL5207 |
| NTR-old | NTR5356 |
| Other | : B1260201523663 |