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GDF-15 and Early Outcomes After LVAD Implantation

Recruitingn/aAges 18 Years - anyAllAkdeniz University
NCT07497308 on ClinicalTrials.gov ↗
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In plain words

What the trial is, and whether it could suit you

This observational study aims to investigate the association between preoperative GDF-15 levels and early postoperative outcomes in patients undergoing left ventricular assist device (LVAD) implantation. The study will evaluate whether elevated preoperative GDF-15 levels are associated with adverse early outcomes, including postoperative complications and mortality. The findings may help improve preoperative risk assessment and identify high-risk patients before LVAD implantation.

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📋 Eligibility rules (as published)
Inclusion Criteria:Adults aged 18 years and older Patients with advanced heart failure undergoing LVAD implantation Availability of preoperative GDF-15 measurement Ability to provide written informed consent or consent provided by a legally authorized representative, according to local regulations - Exclusion Criteria:Age under 18 years Active infection Active malignancy Severe hepatic failure Missing study data Refusal to participate \-
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What it tests

  • Not listed
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Where

1 site
Akdeniz University, Faculty of Medicine, Department of Anesthesiology and Reanimation
Antalya, Turkey (Türkiye)
🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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