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NCT05758194Completed

Mitigating Post-Op RV Dysfunction After LVAD Implantation

Protective Strategies to Mitigate Post-Operative Right Ventricular (PV) Dysfunction After Centrifugal Flow Durable Left Ventricular Assist Device (LVAD) Implantation

Source: ClinicalTrials.gov · Last updated 16 Oct 2025

Brief summary (registry, in English)

This project evaluates right ventricle (RV) protective strategies after left ventricular assist device (LVAD) implantation.

Status (registry)
Completed
Study type
Interventional
Enrollment
20 (actual)
First submitted
24 Feb 2023
Start date
22 Mar 2023
Primary completion date
31 Dec 2024
Lead sponsor
University of Chicago
NCT number
NCT05758194

What you commit to

  • Study type: Interventional
  • Participants enrolled: 20
  • From 22 Mar 2023 to the primary completion date, 31 Dec 2024
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Patients with RV implantable cardiac device (ICD)/pacemaker lead who are pacemaker-dependent

Other

  • Patients with pre-operative right ventricular mechanical circulatory support or having high likelihood of requiring right ventricular mechanical circulatory support.
  • Pregnant patients

Who the study is looking for

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

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
University of Chicago
Coordinator of this site? Confirm its status
ChicagoUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.