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
| Type | Name | Description |
|---|---|---|
| DRUG | Epinephrine Norepinephrine Dobutamine Dopamine Levosimendan | Vasoactive-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.