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NCT Number: NCT07382284

Long-Term Survival After LVAD Implantation in End-Stage Heart Failure

This is a prospective, observational, multi-center cohort study designed to evaluate long-term survival and clinical outcomes in patients with end-stage heart failure undergoing left ventricular assist device (LVAD) implantation.

Patients receiving LVAD implantation as part of routine clinical care will be enrolled and followed for up to 3-5 years. During the study period, data will be collected on baseline characteristics, preoperative medical therapy, intraoperative surgical information, in-hospital course, and long-term postoperative medication use, as well as survival status, major clinical outcomes, LVAD-related complications, and hospital readmissions.

In addition, myocardial tissue samples will be obtained from the left ventricular apex during LVAD implantation surgery. These tissue samples are routinely removed as part of the standard surgical procedure and would otherwise be discarded after pathological examination. Peripheral blood samples will also be collected at predefined time points as part of routine clinical blood testing. No additional surgical procedures or invasive interventions are required for this study.

This study does not involve any experimental treatment or changes to standard medical care. All treatments and follow-up assessments are determined by the treating physicians according to routine clinical practice.

The purpose of this study is to improve understanding of long-term outcomes after LVAD implantation and to explore potential biological factors associated with prognosis in patients with end-stage heart failure.

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Key information

Conditions

End-stage Heart Failure

Sex eligibility

All sexes

Study type

Observational

Primary location

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Adults aged ≥18 years
  • Diagnosis of end-stage heart failure refractory to optimal medical therapy
  • Scheduled to undergo left ventricular assist device (LVAD) implantation as part of routine clinical care
  • Able to provide written informed consent for participation and biospecimen collection
  • Willing and able to comply with study procedures and long-term follow-up
  • Availability of left ventricular apical myocardial tissue obtained during LVAD implantation surgery
  • Availability of peripheral blood samples collected during routine clinical care
  • Patients treated at participating study centers

Exclusion criteria

  • Age <18 years
  • Prior implantation of a durable mechanical circulatory support device
  • Concomitant heart transplantation at the time of index surgery
  • Congenital heart disease requiring complex surgical repair
  • Active systemic infection or sepsis at the time of LVAD implantation
  • Known active malignancy with a life expectancy <1 year
  • Severe non-cardiac comorbidities limiting expected survival to less than 1 year (e.g., advanced liver failure, end-stage renal disease not eligible for renal replacement therapy)
  • Inability or unwillingness to provide informed consent
  • Pregnancy or breastfeeding at the time of enrollment
  • Inadequate quantity or quality of myocardial tissue or peripheral blood samples for planned analyses

Treatment and study plan

Left Ventricular Assist Device (LVAD) implantation

Other

Left ventricular assist device (LVAD) implantation performed as part of routine clinical care for patients with end-stage heart failure. This study is observational in nature and does not assign, alter, or mandate any intervention. The decision to implant an LVAD, the type of device used, perioperative management, and postoperative treatment are determined solely by the treating clinical team according to standard clinical practice.

Other names: Mechanical circulatory support implantation

Primary outcomes

  1. Clinical response after LVAD implantation

    Time frame: During longitudinal follow-up up to 5 years after LVAD implantation

    Patients will be classified as responders or non-responders based on predefined criteria.

Secondary outcomes

  1. Genetic and molecular correlates of clinical response after LVAD implantation

    Time frame: Assessed during follow-up up to 3-5 years after LVAD implantation

    Genetic and molecular analyses will be performed using myocardial tissue obtained from the left ventricular apex during LVAD implantation and peripheral blood samples collected during routine clinical care. Genome-wide association analyses and expression quantitative trait locus (eQTL) analyses will be conducted to explore associations between genetic variation, gene expression profiles, and long-term clinical response after LVAD implantation. These analyses are exploratory and aim to characterize the biological background underlying heterogeneity in myocardial recovery among patients with end-stage heart failure.

Study contacts

Contact information is provided by the study sponsor or research team.

Tuo Pan, M.D

CONTACT

[email protected]

+86 15205160210

Sponsors and collaborators

Lead sponsor

The Affiliated Nanjing Drum Tower Hospital of Nanjing University Medical School

Other

Collaborators

  • First Affiliated Hospital of Harbin Medical University
  • Qianfoshan Hospital
  • Xinhua Hospital of Ili Kazak Autonomous Prefecture
  • Yangzhou University
  • Zhejiang University

Registry information

Official study title

Long-Term Survival After Left Ventricular Assist Device Support (LVAD) Implantation in Patients With End-Stage Heart Failure: A Prospective, Observational, Multi-Center Cohort Study

Important dates

Study start
2022
Primary completion
2028
Study completion
2028
First posted
Feb 2, 2026
Registry last updated
Feb 2, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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