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Ventricular Assist Device (VAD) Research Registry and Blood Sub-Study

S

Spectrum Health Hospitals

Status

Terminated

Conditions

Heart Failure

Study type

Observational

Funder types

Other

Identifiers

NCT05637242
2015-073

Details and patient eligibility

About

This study is meant to predict the outcome of VAD therapy, by forming a VAD registry for quality assessment, research, and real-time monitoring of patients on VAD therapy. The goal is to optimize the use of VAD therapy for patients, to create an online quality measurement tool for VAD treatment, and to create algorithms to estimate the prognosis for patients getting a VAD.

Full description

Patients eligible for VAD are being sampled before surgery for plasma as well as peripheral blood cells. After surgery patients are being sampled again at 24 h and 7 days. Inflammatory response is being monitored on gene expression as well as cell level and on cytokine level in relation to the outcome.

Enrollment

371 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Subject is ≥ 18 years of age
  2. Subject is treated with a VAD at the Butterworth Campus, Spectrum Health.

Exclusion criteria

  1. Subject is less than 18 years of age.
  2. Known prisoners of the state.
  3. Subject is pregnant.
  4. Non- English speaking patients will be excluded from the blood sub-study

Trial contacts and locations

1

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Central trial contact

Stephen C Orey, MS

Data sourced from clinicaltrials.gov

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