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An Observational, multinational Heart Failure disease registry study to identify routine patterns of diagnosis & medical care for patients of acute heart failure as well as treatment type,long term heart failure related clinical events and re-admission rates during the followup period of 3 years.

International Registry to assess mEdical Practice with lOngitudinal obseRvation for Treatment of Heart Failure (REPORT-HF) - REPORT-HF

Status
Active, not recruiting
Phases
Phase 4
Study type
Observational
Source
CTRI
Registry ID
CTRI/2015/01/005389
Enrollment
20000
Registered
2015-01-13
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: null- Characterize HF patients at hospitalization and assess in-hospital and post-discharge eventsâ?? incidence (i.e., cardiac and non-cardiac primary cause of re-hospitalization, mortality)

Interventions

Intervention1: NIL: NIL Control Intervention1: NIL: NIL

Sponsors

Novartis AG
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients eligible for inclusion in this study have to fulfill all of the following criteria: 1)Patients 18 year old, or older for those countries where the adult age is above 18 year of age, hospitalized at the registry sites with primary diagnosis of acute heart failure. Diagnoses will be made by the treating physicians according to local practices and their clinical judgment (i.e., History/examination; Chest X-ray; ECG, Echocardiogram, BNP or NT-proBNP).

Exclusion criteria

Exclusion criteria: Patients eligible for inclusion in this study have to fulfill all of the following criteria: 1. Patients 18 year old, or older for those countries where the adult age is above 18 year of age, hospitalized at the registry sites with primary diagnosis of acute heart failure. Diagnoses will be made by the treating physicians according to local practices and their clinical judgment (i.e., History/examination; Chest X-ray; ECG, Echocardiogram, BNP or NT-proBNP).

Design outcomes

Primary

MeasureTime frame
To identify best practice in the HF treatment, as well as extent of healthcare resources use.Timepoint: every 6 month till 3 years

Secondary

MeasureTime frame
to collect data on health-related quality of life as well as economic and caregiver burdenTimepoint: every 6 month till 3 years

Countries

Argentina, Austria, Chile, China, Colombia, Germany, Greece, India, Malaysia, Norway, Sweden, Switzerland, United Arab Emirates, United Kingdom

Contacts

Public ContactMurugananthan K

Novartis Healthcare Private Limited

murugananthan.k@novartis.com022-24958545

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026