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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00547924
Other study ID # StV 11-2006
Secondary ID
Status Completed
Phase N/A
First received October 22, 2007
Last updated April 9, 2014
Start date April 2006
Est. completion date January 2010

Study information

Verified date April 2014
Source University of Zurich
Contact n/a
Is FDA regulated No
Health authority Switzerland: Swissmedic
Study type Observational

Clinical Trial Summary

Severe hypotension during reperfusion in liver transplantation is a frequent adverse event. Rare data exist so far about pathophysiology of this phenomenon. The exact role of left ventricular function, which might be impaired causing hypotension, has not been elucidated during the period of reperfusion.

Goal of this study is to:

- perform transesophageal echocardiography in order to assess systolic and diastolic left ventricular function during reperfusion

- determine inflammatory mediators in the plasma which could cause left ventricular dysfunction


Recruitment information / eligibility

Status Completed
Enrollment 17
Est. completion date January 2010
Est. primary completion date January 2010
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 75 Years
Eligibility Inclusion criteria:

- Patients on waiting list for liver transplantation.

- Age: 18-75 years.

Exclusion criteria:

- Strictures, tumours and diverticula of the oesophagus.

- History of oesophageal varices with recent bleeding.

- Oesophageal varices and prothrombin time less than 20% or platetlets les than 30000/ml.

- Instable cervical spine.

- Involvement in other studies.

Study Design

Observational Model: Case-Only, Time Perspective: Prospective


Related Conditions & MeSH terms


Intervention

Behavioral:
Transoesophageal echocardiography
Transoesophageal echocardiography in liver transplantation: left ventricular function during reperfusion

Locations

Country Name City State
Switzerland University Hospital Zurich, Institute for Anesthesiology Zurich

Sponsors (1)

Lead Sponsor Collaborator
University of Zurich

Country where clinical trial is conducted

Switzerland, 

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