Mitigating Post-Op RV Dysfunction After LVAD Implantation
This project evaluates right ventricle (RV) protective strategies after left ventricular assist device (LVAD) implantation.
Conditions:
🦠 Heart Failure 🦠 Right Ventricular Dysfunction 🦠 Right Ventricular Failure
🗓️ Study Start (Actual) 22 March 2023
🗓️ Primary Completion (Estimated) April 2024
✅ Study Completion (Estimated) April 2024
👥 Enrollment (Estimated) 20
🔬 Study Type INTERVENTIONAL
📊 Phase NA
Locations:
📍 Chicago, Illinois, United States

📋 Eligibility Criteria

Description

    Inclusion Criteria:

    • * Age ≥ 18 years
    • * Undergoing durable LVAD implantation without plan for perioperative right ventricular mechanical circulatory support

    Exclusion Criteria:

    • * Patients with pre-operative right ventricular mechanical circulatory support or having high likelihood of requiring right ventricular mechanical circulatory support.
    • * Patients with RV implantable cardiac device (ICD)/pacemaker lead who are pacemaker-dependent
    • * Pregnant patients
Ages Eligible for Study: 18 Years to N/A (ADULT, OLDER_ADULT)
Sexes Eligible for Study: ALL
Accepts Healthy Volunteers: No

🗓️ Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

  • First Submitted 24 February 2023
  • First Submitted that Met QC Criteria 24 February 2023
  • First Posted 7 March 2023

Study Record Updates

  • Last Update Submitted that Met QC Criteria 18 December 2023
  • Last Update Posted 19 December 2023
  • Last Verified December 2023