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Study identifier: NCT07272395 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Right Ventricular Function Changes After CIED Implantation: The RIGHT-CIED Study

Condition: Right Ventricular Dysfunction  ·  Sponsor: Istanbul University - Cerrahpasa

PhaseN/A
Planned participants40
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

This study aims to understand how the right side of the heart changes in people who receive an implantable cardiac electronic device (CIED), such as a pacemaker, ICD, or CRT device. The right ventricle (RV) can sometimes be affected after these devices are placed, but the reasons and timing are not well understood. To investigate this, we will examine participants at two time-points: before their device is implanted and again six months later. At each visit, we will assess heart function using echocardiography, a non-contrast cardiac MRI scan, and an ultrasound score of venous congestion called the VEXUS score. We will also take a small blood sample to measure a biomarker called FGF-23, which may reflect changes in heart function. The study does not involve any experimental treatment, and all implanted devices are part of routine medical care. The imaging tests and blood samples are for research purposes only. By comparing the measurements before and after device implantation, we hope to better understand how CIEDs influence right-sided heart function and whether imaging findings are related to changes in blood biomarkers.

This description comes directly from the study's public registry record.

Talk to the study team

SAHRA ASENA BALCIOGLU, MD  ·  +905304433766  ·  sahra.balcioglu@iuc.edu.tr

Always discuss trial participation with your own doctor first.

Locations (1)

Istanbul University-Cerrahpasa Institute of CardiologyIstanbul, FATIH, Turkey (Türkiye)Recruiting

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Source record: clinicaltrials.gov/study/NCT07272395