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NCT05658120

Reperfusion Syndrome and Vasoplegic Syndrome in Liver Transplant Surgery

Completed Last updated 21 February 2023
What this trial tests

trial testing noradrenaline/adrenaline in Postperfusion Syndrome in 246 participants. Completed in 18 February 2023.

Timeline
13 December 2022
Primary endpoint
13 December 2022
18 February 2023

Quick facts

Lead sponsorHospital Universitari Vall d'Hebron Research Institute
StatusCompleted
Study typeOBSERVATIONAL
Enrollment246
Start date13 December 2022
Primary completion13 December 2022
Estimated completion18 February 2023
Sites1 location across Spain

Drugs / interventions tested

Conditions studied

Sponsor

Hospital Universitari Vall d'Hebron Research Institute

Who can join

Adults 18 to 80, any sex, with Postperfusion Syndrome. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The incidence of postreperfusion syndrome (PRS) and vasoplegic syndrome (VS) is unknown, and occasionally can be confused since these syndromes share some hemodynamic characteristics. In these cases, monitoring with Swan Ganz catheter may be useful to make the differential diagnosis. The main outcome was to analyze reperfusion syndrome and vasoplegic syndrome in patients receiving vasoactive support during liver transplant surgery, in terms of incidence, risk factors and postoperative complications.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other Hospital Universitari Vall d'Hebron Research Institute trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05658120.

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