Comparing hemodynamic monitoring techniques during liver transplantation
Official title: "Monitoraggio Emodinamico Intraoperatorio in OLT"
Run by IRCCS Azienda Ospedaliero-Universitaria di Bologna · NCT06703008 · Data updated 2026-11-12
This study is testing two different ways to monitor blood flow during liver transplant surgery to see if one method can help reduce low blood pressure during the operation.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 180 (estimated) |
| Sponsor | IRCCS Azienda Ospedaliero-Universitaria di Bologna Academic / other |
| Locations | 1 site (Bologna, Emilia-Romagna) |
| Status | Recruiting |
| Started | November 1, 2024 |
| Main results expected | January 1, 2026 |
| Study ends | June 1, 2026 |
| Registry record updated | November 25, 2024 |
| Trial ID | NCT06703008 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates for this study are individuals who are candidates for liver transplantation and can provide informed consent.
✕Probably not a fit
Patients with bleeding esophageal varices, bleeding gastro-esophageal ulcers, or gastro-esophageal anomalies may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This clinical trial aims to compare two hemodynamic monitoring techniques during orthotopic liver transplantation (OLT) to determine if one method can reduce intraoperative hypotension time. Participants will be randomized to receive either conventional monitoring with a pulmonary artery catheter or monitoring with transesophageal echocardiography (TEE). The study will evaluate differences in intraoperative hypotension duration and secondary outcomes such as organ dysfunction and mortality. Given the complexities of OLT, effective hemodynamic management is crucial for improving patient outcomes.
Why it matters
Potential benefit: If successful, this study could lead to improved hemodynamic management during liver transplantation, potentially reducing complications and mortality.
How similar studies have gone: While the use of TEE in liver transplantation has increased, this study is among the first randomized controlled trials to evaluate its effectiveness compared to traditional methods.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Candidate for Liver Transplantation * Acceptance of informed consent to participate in the study. Exclusion Criteria: * Bleeding esophageal varices * Bleeding gastro-esophageal ulcer * Gastro-esophageal anomalies (congenital, acquired or post-surgical)
Where it's running
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IRCSS AOU di Bologna
Bologna, Emilia-Romagna, Italy Recruiting
Study contacts
- Principal investigator: Amedeo Bianchini, MD — IRCCS Azienda Ospedaliero-Universitaria di Bologna
- Study coordinator: Amedeo Bianchini, MD
- Email: amedeo.bianchini@aosp.bo.it
- Phone: 051 2143101
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.