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Clinical Trials/NCT01073345
NCT01073345
Unknown
Not Applicable

Portal Venous Hemodynamic Changes After Hepatectomy and the Incidence of Postoperative Ascites

Heidelberg University1 site in 1 country110 target enrollmentFebruary 2010

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Ascites
Sponsor
Heidelberg University
Enrollment
110
Locations
1
Primary Endpoint
Postoperative ascites
Last Updated
16 years ago

Overview

Brief Summary

The aim of this study is to investigate the pathophysiological mechanisms underlying the formation of posthepatectomy ascites with a focus on the significance of changes in portal venous hemodynamics after hepatic resection. By evaluation of other factors that may be involved in the formation of ascites this study may help to show to what extent the increase of portal venous pressure contributes to ascites formation. Detailed knowledge about pathogenetic factors concerning the formation of postoperative ascites might help preventing protracted hospital stay and further inconveniences to the patient.

Detailed Description

The mechanisms underlying the development of large-volume ascites after hepatectomy remain poorly understood. While studies on animal models suggest an increase of portal venous pressure after hepatectomy that may in turn favor the transudation of fluid into the peritoneal cavity further factors may be critically involved in the postoperative formation of ascites. These factors may include a drop in serum protein levels (and colloid osmotic pressure), a transient impairment in renal function and a surgery-induced capillary leakage. However, a better knowledge of the pathophysiology represents the prerequisite for efficient treatment. In the present study the impact of changes in hepatic hemodynamics after hepatectomy on development of ascites will be investigated. Enrolled patients will receive measurement of portal venous flow and pressure as well as hepatic artery flow before and after hepatic resection. Associations of changes in these parameters with development of postoperative ascites and further postoperative complications will be evaluated.

Registry
clinicaltrials.gov
Start Date
February 2010
End Date
December 2010
Last Updated
16 years ago
Study Type
Observational
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Patients scheduled for elective hepatic resection
  • Age equal or greater than 18 years
  • Informed consent

Exclusion Criteria

  • Evidence of ascites or hypalbuminemia preoperatively
  • Renal insufficiency
  • Expected lack of compliance
  • Impaired mental state or language problems

Outcomes

Primary Outcomes

Postoperative ascites

Time Frame: 7 days

Study Sites (1)

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