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Saline
25% albumin for Complications of Liver Transplant
Phase 4
Waitlist Available
Led By Sheldon Magder, MD
Research Sponsored by McGill University Health Centre/Research Institute of the McGill University Health Centre
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 30 and 60 minutes after infusion
Awards & highlights
Study Summary
The primary aim of this study is to assess the effect of hyperoncotic albumin on vascular hemodynamics and oxygen delivery after orthotopic liver transplant. The secondary aim is to try to identify the dominant physiological mechanism so that we will be able to better identify patients that may benefit from the use of albumin (25%) boluses in addition to standard care in patients following liver transplantation.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 60 minutes after the infusion of the fluid
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~60 minutes after the infusion of the fluid
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Cardiac index (CI)
Secondary outcome measures
A decrease in leak and plasma expansion
Cardiac function response
Cardiac output response
+1 moreTrial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: 25% albuminExperimental Treatment1 Intervention
Group II: SalineActive Control1 Intervention
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Who is running the clinical trial?
McGill University Health Centre/Research Institute of the McGill University Health CentreLead Sponsor
442 Previous Clinical Trials
159,154 Total Patients Enrolled
Sheldon Magder, MDPrincipal InvestigatorMcGill University Health Centre/Research Institute of the McGill University Health Centre
Frequently Asked Questions
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