Clinical Trials Directory

Trials / Completed

CompletedNCT05702333

Vasoactive-inotropic Support and Levosimendan Use After Lung Transplantation

Postoperative Prolonged Vasoactive-inotropic Support and Levosimendan Use After Lung Transplantation: a Retrospective Analysis of Risk Factors and Impact on Outcomes

Status
Completed
Phase
Study type
Observational
Enrollment
150 (actual)
Sponsor
Policlinico Hospital · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Bilateral Lung transplantation (LUTX) is performed in selected patients with end-stage respiratory failure. During surgery, pulmonary arteries are sequentially cross-clamped. This can cause acute heart failure and hemodynamic instability that eventually persist into the postoperative period, leading to the need for prolonged vasoactive support in the postoperative Intensive Care Unit. Levosimendan is a relatively new vasoactive-inotropic drug, with different pharmacodynamic properties. This observational retrospective cohort study primarily aims 1) to describe the need for prolonged vasoactive support; 2) to evaluate the risk factors for prolonged vasoactive support; 3) to assess the impact of prolonged vasoactive support on outcomes. The secondary aim is to describe the use of Levosimendan in this cohort of patients.

Conditions

Interventions

TypeNameDescription
DRUGEpinephrine Norepinephrine Dobutamine Dopamine LevosimendanVasoactive-inotropic drugs were administered according to clinical decision of the doctor in charge.

Timeline

Start date
2017-02-01
Primary completion
2022-07-31
Completion
2022-07-31
First posted
2023-01-27
Last updated
2023-04-05

Locations

1 site across 1 country: Italy

Source: ClinicalTrials.gov record NCT05702333. Inclusion in this directory is not an endorsement.