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NCT05881278Active, not recruiting

XVIVO Heart Perfusion System (XHPS) With Supplemented XVIVO Heart Solution (SXHS)

PRESERVE Heart Study: A Prospective, Multi-center, Single-Arm, Open-Label Study of Hearts Transplanted After Non-Ischemic Heart PRESERVation From Extended Donors

Source: ClinicalTrials.gov · Last updated 17 Aug 2026

Brief summary (registry, in English)

The purpose of this study is to evaluate if Non-Ischemic Heart Preservation (NIHP) of extended criteria donor hearts using the XVIVO Heart Preservation System (XHPS) is a safe and effective way to preserve and transport hearts for transplantation.

Status (registry)
Active, not recruiting
Study type
Interventional
Enrollment
141 (estimated)
First submitted
18 May 2023
Start date
10 Oct 2023
Primary completion date
22 Nov 2025
Lead sponsor
XVIVO Perfusion
NCT number
NCT05881278

What you commit to

  • Study type: Interventional
  • Planned participants: 141
  • From 10 Oct 2023 to the primary completion date, 22 Nov 2025
  • 20 sites 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.

Criteria the registry did not label

  • Recipient Inclusion Criteria:
  • Age ≥18 years.
  • Signed informed consent form (ICF).
  • Listed for heart transplantation
    • Recipient Exclusion Criteria:
  • Previous solid organ or bone marrow transplantation.
  • Requires a multi-organ transplant.
  • Subject is enrolled and ongoing in another investigational pharmaceutical or medical device clinical trial (Exception: observational studies are permitted).
  • Subject is on mechanical circulatory support pre-transplant other than durable LVAD, Impella or intra-aortic balloon pump.
  • History of complex congenital heart disease ie: single ventricle physiology (Per Investigators discretion).
  • Subject on renal replacement therapy/dialysis.
  • Ventilator dependence (subject is intubated at time of transplant/unable to provide consent or re-affirmation of consent).
  • Sensitized subject is undergoing desensitization treatment.
    • Donor Inclusion Criteria:
  • Estimated Cross Clamp Time ≥ 4 hours, OR
  • Estimated Cross Clamp Time ≥ 2 hours, AND
    • Any ONE or more of the following:
    • Age ≥ 50 years
    • LVEF 40-50% at time of provisional acceptance
    • Down-time ≥ 20 mins
    • Hypertrophy/Septal thickness \>12- ≤16mm
    • Angiographic luminal irregularities with no significant CAD, OR
  • Donation after Circulatory Death (DCD) donors.
    • Donor Exclusion Criteria:
  • Unstable hemodynamics requiring high-dose inotropic support.
  • Significantly abnormal coronary angiogram defined as CAD \> 50% stenosis of one or more vessels.
  • Moderate to severe cardiac valve pathology.
  • Investigator's clinical decision to exclude from trial.
  • Previous Sternotomy.

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

Full criteria on ClinicalTrials.gov

Sites (20)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Emory University
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AtlantaUnited StatesUnknown status
Johns Hopkins Medicine
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BaltimoreUnited StatesUnknown status
University of Maryland Medical Center/University of Maryland, Baltimore
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BaltimoreUnited StatesUnknown status
Northwestern Memorial Hospital
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ChicagoUnited StatesUnknown status
Cleveland Clinic Foundation
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ClevelandUnited StatesUnknown status
Ohio State University
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ColumbusUnited StatesUnknown status
UT Southwestern Medical Center
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DallasUnited StatesUnknown status
Duke University
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DurhamUnited StatesUnknown status
University of California San Diego
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La JollaUnited StatesUnknown status
David Geffen School of Medicine at UCLA
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Los AngelesUnited StatesUnknown status
Cedars Sinai
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Los AngelesUnited StatesUnknown status
Vanderbilt University
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NashvilleUnited StatesUnknown status
Columbia University Irving Medical Center/New York Presbyterian Hospital
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New YorkUnited StatesUnknown status
NYU Langone Health
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New YorkUnited StatesUnknown status
University of Nebraska Medical Center
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OmahaUnited StatesUnknown status
Stanford Medicine
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Palo AltoUnited StatesUnknown status
University of Pittsburgh Medical Center
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PittsburghUnited StatesUnknown status
University of Washington Medical Center
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SeattleUnited StatesUnknown status
Washington University (Barnes-Jewish Hospital)
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St LouisUnited StatesUnknown status
Montefiore Medical Center
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The BronxUnited StatesUnknown status

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