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Upper Extremity Function in Patients With Reduced Ejection Fraction Heart Failure and Cardiac Implantable Electronic Devices

NCT07253909 · Status: ENROLLING_BY_INVITATION · Type: OBSERVATIONAL · Enrollment: 72

Last updated 2025-11-28

No results posted yet for this study

Summary

The aim of this study is to evaluate in detail the factors that determine upper extremity function, determine its effect on prognosis, hospital admission, hospitalization, and mortality, and examine the results according to the use of different implantable cardiac implantable electronic devices.

Conditions

  • Heart Failure
  • Implantable Cardioverter Defibrillator (ICD)
  • Cardiac Resynchronisation Therapy (CRT)
  • Reduced Ejection Fraction Heart Failure

Interventions

OTHER

Not applicable- observational study

Not applicable- observational study

Sponsors & Collaborators

  • Hacettepe University

    lead OTHER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-05-30
Primary Completion
2026-08-30
Completion
2027-05-30

Countries

  • Turkey (Türkiye)

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07253909 on ClinicalTrials.gov