Actively Recruiting

Age: 65Years +
All Genders
NCT03209414

Frailty Syndrome in Daily Practice of Interventional Cardiology Ward

Led by Medical University of Silesia · Updated on 2023-04-12

1000

Participants Needed

1

Research Sites

554 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The impact of frailty on immediate and long term outcomes of invasive treatment of coronary artery disease is not fully characterized. The assessment of frailty may help physicians in the selection of best treatment option and in the timing and modality of the follow-up. The FRAilty syndrome in daily Practice of Interventional CArdiology ward (FRAPICA) study is designed with the aim to validate the use of the Fried frailty scale and instrumental activities of daily living scale (IADL) as prognostic tools in patients admitted to hospital for symptomatic coronary artery disease, either stable, unstable, or acute coronary syndrome (ACS). The FRAPICA study is a single center prospective study enrolling patients aged ≥65 years. The aims are (1) to describe Fried frailty scale and IADL scale distribution before hospital discharge and (2) to investigate the prognostic role of Fried frailty and IADL scores. The outcomes are: (1) results of invasive treatment, (2) its complications (periinterventional MI, contrast-induced nephropathy, blood loss), (3) three-year all-cause mortality, cardiovascular mortality, stroke, myocardial infarction, reintervention, heart failure, hospital readmission for any cause, and a composite of the above mentioned. Ancillary analyses will be focused on different clinical presentations, different tools to assess frailty and risk stratification. The FRAPICA program will fill critical gaps in the understanding of the relation between frailty, cardiovascular disease, interventional procedures and outcome. It will enable more personalized risk assessment and identification of new targets for interventions.

CONDITIONS

Official Title

Frailty Syndrome in Daily Practice of Interventional Cardiology Ward

Who Can Participate

Age: 65Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Aged 65 years or older
  • Diagnosed with symptomatic coronary artery disease including stable, unstable, NSTEMI, or STEMI
  • Able to provide written, informed consent
Not Eligible

You will not qualify if you...

  • Lack of consent to participate in the study

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

II Dept. of Cardiology in Zabrze Medical University of Silesia

Zabrze, Upper Silesia, Poland, 41-800

Actively Recruiting

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Research Team

A

Andrzej R Tomasik, M.D. Ph.D., FESC

CONTACT

E

Ewa Nowalany-Kozielska, Prof.

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

4

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Frailty Syndrome in Daily Practice of Interventional Cardiology Ward | DecenTrialz