Status:

COMPLETED

Portal Pressure Effects of Phlebotomy Combined to Vasopressin Use in Cirrhotic Patients Undergoing Liver Transplantation

Lead Sponsor:

Centre hospitalier de l'Université de Montréal (CHUM)

Conditions:

Liver Transplantation

Portal Hypertension

Eligibility:

All Genders

18+ years

Brief Summary

Liver transplantation is the standard treatment for chronic advanced liver disease, whether or not associated with a primary liver tumor. The intraoperative bleeding and the need for blood transfusion...

Detailed Description

METHODS Objectives The primary objective will be to measure the hemodynamic effects of vasopressin on portal pressure in cirrhotic patients who have had a hypovolemic phlebotomy during a liver trans...

Eligibility Criteria

Inclusion

  • Cirrhotic patients undergoing a liver transplantation
  • 18 years and older
  • Planned use of vasopressin during the surgery

Exclusion

  • Fulminant or sub-fulminant hepatitis without underlying chronic liver disease
  • Anesthetic plan does not include the use of vasopressin (contraindication or not relevant according to the anesthesiologist)

Key Trial Info

Start Date :

August 24 2020

Trial Type :

OBSERVATIONAL

Allocation :

ACTUAL

End Date :

July 6 2022

Estimated Enrollment :

60 Patients enrolled

Trial Details

Trial ID

NCT04472312

Start Date

August 24 2020

End Date

July 6 2022

Last Update

July 22 2022

Active Locations (1)

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Centre Hospitalier de l'Université de Montréal (CHUM)

Montreal, Quebec, Canada, H2X 3E4