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
- Diseases
- Heart failure
- 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
Sites (20)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Emory University Coordinator of this site? Confirm its status | Atlanta | United States | Unknown status |
| Johns Hopkins Medicine Coordinator of this site? Confirm its status | Baltimore | United States | Unknown status |
| University of Maryland Medical Center/University of Maryland, Baltimore Coordinator of this site? Confirm its status | Baltimore | United States | Unknown status |
| Northwestern Memorial Hospital Coordinator of this site? Confirm its status | Chicago | United States | Unknown status |
| Cleveland Clinic Foundation Coordinator of this site? Confirm its status | Cleveland | United States | Unknown status |
| Ohio State University Coordinator of this site? Confirm its status | Columbus | United States | Unknown status |
| UT Southwestern Medical Center Coordinator of this site? Confirm its status | Dallas | United States | Unknown status |
| Duke University Coordinator of this site? Confirm its status | Durham | United States | Unknown status |
| University of California San Diego Coordinator of this site? Confirm its status | La Jolla | United States | Unknown status |
| David Geffen School of Medicine at UCLA Coordinator of this site? Confirm its status | Los Angeles | United States | Unknown status |
| Cedars Sinai Coordinator of this site? Confirm its status | Los Angeles | United States | Unknown status |
| Vanderbilt University Coordinator of this site? Confirm its status | Nashville | United States | Unknown status |
| Columbia University Irving Medical Center/New York Presbyterian Hospital Coordinator of this site? Confirm its status | New York | United States | Unknown status |
| NYU Langone Health Coordinator of this site? Confirm its status | New York | United States | Unknown status |
| University of Nebraska Medical Center Coordinator of this site? Confirm its status | Omaha | United States | Unknown status |
| Stanford Medicine Coordinator of this site? Confirm its status | Palo Alto | United States | Unknown status |
| University of Pittsburgh Medical Center Coordinator of this site? Confirm its status | Pittsburgh | United States | Unknown status |
| University of Washington Medical Center Coordinator of this site? Confirm its status | Seattle | United States | Unknown status |
| Washington University (Barnes-Jewish Hospital) Coordinator of this site? Confirm its status | St Louis | United States | Unknown status |
| Montefiore Medical Center Coordinator of this site? Confirm its status | The Bronx | United States | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.