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GDF-15 and Early Outcomes After LVAD Implantation

Association of Preoperative GDF-15 Levels With Early Postoperative Outcomes and Mortality After LVAD Implantation

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07497308
Acronym
LVAD-GDF15
Enrollment
48
Registered
2026-03-27
Start date
2026-02-04
Completion date
2026-12-23
Last updated
2026-03-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Advanced Heart Failure, Left Ventricular Assist Device Implantation

Keywords

Left Ventricular Assist Device, GDF-15, Postoperative Outcomes, Early Mortality

Brief summary

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.

Detailed description

Left ventricular assist device (LVAD) implantation is an established treatment option for patients with advanced heart failure. However, these patients remain at substantial risk for early postoperative morbidity and mortality. Identification of preoperative biomarkers associated with adverse outcomes may improve perioperative risk assessment and support clinical decision-making. Growth differentiation factor-15 (GDF-15) is a biomarker related to inflammation, oxidative stress, and cardiovascular injury, and may have prognostic value in high-risk cardiac populations. This observational study will investigate the relationship between preoperative GDF-15 levels and early postoperative outcomes in patients undergoing LVAD implantation. Preoperative serum GDF-15 levels will be evaluated for their association with early postoperative complications, mortality, and other short-term clinical outcomes. The study is intended to clarify whether GDF-15 can serve as a useful biomarker for identifying patients at increased risk before LVAD implantation. Improved preoperative risk stratification may help optimize perioperative management and patient selection.

Interventions

None listed

Sponsors

Akdeniz University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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 \-

Design outcomes

Primary

MeasureTime frameDescription
Early Postoperative Mortality30 days after LVAD implantationMortality occurring during the early postoperative period after LVAD implantation

Secondary

MeasureTime frameDescription
Postoperative ComplicationsUp to 30 days after LVAD implantationOccurrence of early postoperative complications after LVAD implantatio

Countries

Turkey (Türkiye)

Contacts

CONTACTemel gündüz, md
dregunduz@hotmail.com+902422496000

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 28, 2026