GDF-15 levels to predict early outcomes after LVAD implantation
Official title: Association of Preoperative GDF-15 Levels With Early Postoperative Outcomes and Mortality After LVAD Implantation
Run by Akdeniz University · NCT07497308 · Data updated 2026-11-12
We will see if pre-surgery blood levels of GDF-15 can predict early complications or death in adults having an LVAD implanted.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 48 (estimated) |
| Sponsor | Akdeniz University Academic / other |
| Locations | 1 site (Antalya, Please Select:) |
| Status | Recruiting |
| Started | February 4, 2026 |
| Main results expected | August 10, 2026 |
| Study ends | December 23, 2026 |
| Registry record updated | March 27, 2026 |
| Trial ID | NCT07497308 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults aged 18 or older with advanced heart failure who are scheduled for LVAD implantation and can provide a preoperative blood sample and informed consent.
✕Probably not a fit
Patients under 18, those with active infection, active malignancy, severe hepatic failure, or missing required data are unlikely to benefit from GDF-15–based risk information in this project.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This observational study will enroll adults with advanced heart failure who are scheduled to receive a left ventricular assist device at Akdeniz University. Preoperative serum GDF-15 will be measured and patients will be followed through the early postoperative period to record complications, mortality, and other short-term clinical outcomes. Statistical analyses will examine whether higher preoperative GDF-15 is associated with greater risk of early adverse events after LVAD surgery. The goal is to determine whether GDF-15 could improve preoperative risk stratification and inform perioperative management.
Why it matters
Potential benefit: If successful, preoperative GDF-15 measurement could help identify patients at higher risk for early complications or death and guide perioperative planning to improve outcomes.
How similar studies have gone: Previous research in heart failure and cardiac surgery populations has suggested GDF-15 has prognostic value, but its specific use for predicting early LVAD outcomes remains relatively untested.
Who can join: the full rules
Show full inclusion / exclusion criteria
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 \-
Where it's running
-
Akdeniz University, Faculty of Medicine, Department of Anesthesiology and Reanimation
Antalya, Please Select:, Turkey (Türkiye) Recruiting
Study contacts
- Study coordinator: emel gündüz, md
- Email: dregunduz@hotmail.com
- Phone: +902422496000
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.