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MBT in liver disease for Tricuspid Atresia (MBT+Fontan Trial)
N/A
Waitlist Available
Led By Daniel R Ganger, MD
Research Sponsored by Northwestern University
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 1 year
Awards & highlights
MBT+Fontan Trial Summary
This trial will assess a non-invasive functional liver test in patients with the Fontan circulation that may be used for prognostic purposes.
Eligible Conditions
- Tricuspid Atresia
- Dilated Cardiomyopathy
MBT+Fontan Trial Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 1 year
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~1 year
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
MR Elastography Results Compared to Methacetin Breath Test Results in Patients Undergoing Heart and Liver Transplant Evaluation.
Methacetin Breath Test Results in Patients Undergoing Heart and Liver Transplant Evaluation.
To Explore Any Association Between MBT Parameter and Clinical Parameters Already Available Per Standard of Care in Patients Undergoing Heart and Liver Transplant Evaluation.
MBT+Fontan Trial Design
1Treatment groups
Experimental Treatment
Group I: MBT in liver diseaseExperimental Treatment1 Intervention
Methacetin Breath test (MBT) intervention. We will use the MBT test to measure time from administration of 13C methacetin to obtaining the peak elimination of 13CO2.
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Who is running the clinical trial?
Northwestern UniversityLead Sponsor
1,600 Previous Clinical Trials
915,508 Total Patients Enrolled
Daniel R Ganger, MDPrincipal InvestigatorNorthwestern University
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