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The Türkiye Heart Failure Registry

The Türkiye Heart Failure (TURK-HF) Registry

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06707220
Acronym
TURK-HF
Enrollment
5000
Registered
2024-11-27
Start date
2025-01-08
Completion date
2027-12-31
Last updated
2025-03-03

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

Conditions

Heart Failure

Brief summary

A comprehensive understanding of the socio-demographic, clinical, and biological characteristics of patients with heart failure is essential to develop novel strategies for improving outcomes. The identification of the barriers to guideline-directed medical therapy implementation in a real-world setting is critical to decreasing the risk of heart failure hospitalization and mortality. A comprehensive and well-designed heart failure registry can determine the clinical characteristics of patients with heart failure, identify patient, physician, and healthcare system-related factors for the non-use of evidence-based therapies, and improve the implementation of guideline-directed medical therapy. It should be noted that the number of heart failure registries that enroll patients with de novo heart failure, chronic heart failure (outpatients), and worsening of heart failure (hospitalized or treated in the emergency department), with all three relevant ejection fraction categories (heart failure with reduced ejection fraction, heart failure with mildly-reduced ejection fraction, and heart failure with preserved ejection fraction), is limited. Furthermore, only a few registries assess detailed aspects of guideline adherence, treatment decisions, and both in-hospital and long-term outcomes. Therefore, the Türkiye Heart Failure (TURK-HF) registry has been designed to address this gap in knowledge about the identification, management, and long-term prognosis of patients with heart failure in a real-world setting.

Interventions

Treated with optimal guideline-directed medical therapy

Sponsors

Baskent University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

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

Inclusion criteria

Presence of heart failure -

Exclusion criteria

Age \<18 years \-

Design outcomes

Primary

MeasureTime frame
Heart failure hospitalizationFrom enrollment to the end of follow-up period at 12 months
Cardiovascular mortalityFrom enrollment to the end of follow-up period at 12 months
Composite of heart failure hospitalization and cardiovascular mortalityFrom enrollment to the end of follow-up period at 12 months

Secondary

MeasureTime frame
All-cause mortalityFrom enrollment to the end of follow-up period at 12 months

Countries

Turkey (Türkiye)

Contacts

Primary ContactUmut Kocabaş
umutkocabas@hotmail.com+905079974999

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026