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Observational study to predict readmission for heart failure patients

An observational study to assess & predict the in-patient course, risk of readmission and mortality for patients hospitalised for or with Heart Failure

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ISRCTN
Registry ID
ISRCTN96643197
Enrollment
1000
Registered
2013-04-18
Start date
2012-09-27
Completion date
Unknown
Last updated
2021-04-12

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

Conditions

Topic: Cardiovascular

Interventions

Development of risk model, Identifying the Nature of Risk and Developing Prediction Models 1. To develop one or more multi-dimensional risk stratification models to identify patients w

Sponsors

Hull and East Yorkshire Hospitals NHS Trust
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Inclusion Criteria for the Risk Stratification Component: 1. Age >18 years 2. In hospital 3. Usual residence is in the catchment region for Hull & East Yorkshire Hospitals Trust (this enables efficient follow-up) 4. Either 4.1. Treated with loop diuretics Or 4.2.Clinical diagnosis of heart failure 5. Willing and able to provide informed consent Additional Inclusion Criteria for the Monitoring Component of the Study: Heart failure as a dominant diagnosis meaning that 1. There is objective evidence of cardiac dysfunction as evidenced by a least ONE of the following: 1.1. Left ventricular ejection fraction 4.0 cm (or >2.5 cm/m in height) 1.3. NT ? ProBNP > 400pg/ml (>47.3pmol/L (or BNP >150 pg/ml) if in sinus rhythm or >1,200pg/ml (or BNP >450pg/ml) if in atrial fibrillation 2. The patient is receiving loop diuretics 3. Target Gender: Male & Female ; Lower Age Limit 80 years

Exclusion criteria

Exclusion criteria: Unable to understand and comply with protocol or to give informed consent. There are no other exclusion criteria for the risk stratification study. Additional Exclusion Criteria for the Monitoring Component of the Study: The duration of admission is likely to be determined by the need for treatment other than for heart failure (for instance, patients with infective endocarditis, major stroke disability or major cognitive impairment will be excluded).

Design outcomes

Primary

MeasureTime frame
The proportion of patients with an ?optimal length of stay?; Timepoint(s): Discharge.

Secondary

MeasureTime frame
No secondary outcome measures

Countries

United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 23, 2026