AzTrials
AzTrials

Heart FailureGRASP-HFNCT06469814

Snapshot Study on Patients With Heart Failure

An observational study of Heart Failure, run by European Society of Cardiology at 63 sites in 11 countries.

Enrolling by invitation

Enrolling by invitation. The study team selects and invites participants, usually from an existing group of patients.

Sites and contacts
Official record

Search all trials

Trial summary

The goal of this observational study is to provide a better understanding of medical practice for heart failure management based on real-world data, collected both across Europe and the rest of the world, using robust methodology and representativeness within each country. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Heart Failure
How many people
4,000 participants
Where
63 sitesin 11 countries
Study dates
27 Sep 2024to Jul 2029
How long will I take part?
6 Months
Phase
Observational

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: The study population is all consenting patients seen in the outpatient clinic for chronic HF and all consenting patients admitted for acute HF in the study center as their standard medical care.

Who may be able to join

  • Adult patients with chronic or acute Heart Failure (HF), regardless of ejection fraction, either:
  • Outpatient with chronic HF (including first-time diagnosis), according to the clinical judgment.
  • OR
  • Patients admitted to hospital or presenting to Emergency Department or Acute out-patient care for acute HF for whom an IV (diuretics, inotropes, vasodilators) or mechanical therapy for HF (mechanical circulatory support) is administered.

Who cannot join

  • Age <18 years
  • Patients unwilling to consent (or patient's legally authorized representative unwilling to consent, if the patient is unable to consent).

Trial locations and contacts

63 sites in 11 countries. Contact the study team or a site near you to ask about taking part.

63 sites in 11 countries

Czechia16 sites
  • ICRC, St. Anne's University Hospital

    Brno

  • EDUMED, Kardiologická ambulance Broumov

    Broumov

  • České Budějovice Hospital

    České Budějovice

  • Kardio Dodulík s.r.o.

    Havířov

  • EDUMED, Kardiologická ambulance Hradec Králové

    Hradec Králové

  • EDUMED, Kardiologická ambulance Jaroměř

    Jaroměř

  • Charles University and University Hospital

    Motol

  • EDUMED, Kardiologická ambulance Náchod

    Náchod

  • University Hospital Ostrava

    Ostrava

  • Krajska nemocnice Pardubice

    Pardubice

  • Kardiologie v sadech

    Pilsen

  • University Hospital and Faculty of Medicine Pilsen, Charles University

    Pilsen

  • IKEM Prague

    Prague

  • Na Homolce Hospital

    Prague

  • University hospital Vinohrady

    Prague

  • Všeobecná fakultní nemocnice (General University Hospital)

    Prague

Other trials in Czechia

Azerbaijan12 sites
  • Azerbaijan Medical University

    Baku

  • Baku Health Center

    Baku

  • Baku Medical plaza Central Hospital

    Baku

  • Central Clinic Hospital

    Baku

  • Educational Therapeutical Hospital of Azerbaijan Medical University

    Baku

  • Medi Style Hospital

    Baku

  • Republican Clinical Hospital

    Baku

  • Scientific Research Institute of Cardiology

    Baku

  • Zeferan Hospital

    Baku

  • Ganja Cardiology Hospital

    Ganja

  • Nakhchivan Military Hospital

    Nakhchivan

  • ER Medical

    Xaçmaz

Other trials in Azerbaijan

Belgium10 sites
  • OLV Hospital

    Aalst

  • Hôpital Universitaire de Bruxelles - Hôpital Erasme

    Brussels

  • Saint Luc Brussels

    Brussels

  • AZ Sint Blasius

    Dendermonde

  • Ziekenhuis Oost-Limburg

    Genk

  • AZ Maria Middelares

    Ghent

  • Jessa Hospital

    Hasselt

  • AZ Groeninge

    Kortrijk

  • UZ Gasthuisberg Leuven

    Leuven

  • CHU UCL Namur

    Yvoir

Other trials in Belgium

Bosnia and Herzegovina5 sites
  • University Clinical Center of Republic of Srpska

    Banja Luka

  • Cantonal Hospital Bihac

    Bihać

  • Clinical Center University of Sarajevo

    Sarajevo

  • General Hospital 'Prim. Dr. Abdulah Nakas

    Sarajevo

  • General hospital East Sarajevo

    Sarajevo

Other trials in Bosnia and Herzegovina

Armenia4 sites
  • Astghik Medical Center

    Yerevan

  • Erebouni Medical Center

    Yerevan

  • Nork Marash Medical Center

    Yerevan

  • Yerevan State Medical University (YSMU) University Hospital N1

    Yerevan

Other trials in Armenia

Bulgaria4 sites
  • Multiprofile Hospital for Active Treatment "Heart and Brain"

    Sofia

  • University Multiprofile Hospital for Active Treatment "Sv. Georgi" EAD

    Sofia

  • MHAT Trakiya

    Stara Zagora

  • UMHAT "St Marina"

    Varna

Other trials in Bulgaria

Bhutan3 sites
  • Central Regional Referral Hospital

    Geylegphug

  • Eastern Regional Referral Hospital Mongar

    Mongar

  • Jigme Dorji Wangchuck National Referral Hospital

    Thimphu

Cyprus3 sites
  • CardioHealth Center

    Nicosia

  • Nicosia General Hospital

    Nicosia

  • Panayiotidescardio clinic

    Nicosia

Other trials in Cyprus

Austria2 sites
  • University Heart Center Graz

    Graz

  • University Hospital Salzburg

    Salzburg

Other trials in Austria

Croatia2 sites
  • University Hospital of Split

    Split

  • Clinical Hospital Dubrava

    Zagreb

Other trials in Croatia

United Arab Emirates2 sites
  • Dubai Hospital

    Dubai Healthcare City

  • Rashid Hospital

    Dubai Healthcare City

Other trials in United Arab Emirates

About this study

Official title: Global Registries And Surveys Programme - Heart Failure Snapshot Study (GRASP-HF)

The goal of this observational study is to provide a better understanding of medical practice for heart failure management based on real-world data, collected both across Europe and the rest of the world, using robust methodology and representativeness within each country.

Standard management of patients will be the diagnostic and therapeutic interventions routinely performed in each center for patients presenting with signs and symptoms of chronic/acute heart failure.

Read the detailed description

Information collected by the GRASP-HF study assesses adherence to the ESC HF Guidelines focusing on Quality Indicators, in both chronic and acute HF.

For that reason, the GRASP-HF snapshot study is evolving in parallel with the long-term Heart Failure Association initiative - ICARe-HF: the Improving Care through Accreditation and Recognition in Heart Failure (ICARe-HF) programme. ICARe-HF is an international accreditation programme for heart failure centres which is about improving patient outcomes by raising standards in care facilities and recognising those that apply best practices. The GRASP-HF snapshot study serves to verify the performance of individual centres through data collection of real-world patient data.

Conditions
Heart Failure
Medical subject headings
Heart Failure

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

Study groups in NCT06469814
Study groupRoleWhat they receive
Patients with chronic heart failureNot described
Patients with acute heart failureNot described

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Adherence to ESC Guidelines in Heart Failure 2021

    Full adherence to guidelines for heart failure management

    Measured: 12 months per site

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted24 Jun 2024
  2. Study start27 Sep 2024
  3. Primary completion30 Jul 2025
  4. Study completionJul 2029 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
4,000 participants (estimated)
Target duration
6 Months
IDs, dates and publications
ClinicalTrials.gov ID
NCT06469814
Sponsor's protocol ID
GRASP-HF
Acronym
GRASP-HF
Status last verified
Aug 2026
First submitted
17 Jun 2024
Last updated
20 Aug 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Free account

Keep searching with a free account

You’ve used your 3 free searches for this session. Log in or create a free AzTrials account to keep searching clinical trials and save the ones you want to follow.

Create a free accountLog in