Management of Heart Failure in Italian Outpatients Clinics: Observational Study (OPTIMA-HF)

  • STATUS
    Recruiting
  • participants needed
    4000
  • sponsor
    Federico II University
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Updated on 15 March 2024
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Summary

OPTIMA-HF is an observational, cross-sectional, multicenter, real-life study conducted in two different clinical settings: HF outpatients' clinics of Italian University Hospitals and territorial Cardiology outpatients' services.

Aim of the Optimization of Therapy in the Italian Management of Heart Failure [OpTIMa-HF] Registry is to collect data on HF patients followed in different Italian outpatients' settings to describe the current Italian population of HF patients, in terms of demographic characteristics and disease features, with a specific focus on guideline-directed medical therapy (GDMT) prescription, assessing its improvement after educational activities. In the present analysis we report the baseline data on the general enrolled population with a specific focus on HFrEF treatment adherence and prescription rates, according to the most recent European Guidelines.

Details
Condition Heart Failure
Age 18years or above
Treatment data collection
Clinical Study IdentifierNCT06287164
SponsorFederico II University
Last Modified on15 March 2024

Eligibility

 Yes No Not Sure

Inclusion Criteria

age >18 years, post-menopausal, permanent sterile, or
childbearing
potential on highly effective contraceptive methods women, stable clinical conditions (NYHA
class I-III), outpatients setting, capability to understand the study procedures and sign
the informed consent form

Exclusion Criteria

any clinical condition that would have jeopardized patient safety while
participating in this study
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How to participate?

Step 1 Connect with a study center

Since this trial requires contact information verification, you will receive an email with the information you provided asking for your validation. Only after this verification step your referral will be sent to the study site selected.

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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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