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Fibroscan for Non-invasive Indices to Predict Hepatic Fibrosis in BA Patients.

N/A
Waitlist Available
Led By Lawrence Worobetz, MD
Research Sponsored by University of Saskatchewan
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
-Any outpatient undergoing routine pacemaker interrogation at pacemaker clinic
Timeline
Screening 3 weeks
Treatment Varies
Follow Up up to 5 years
Awards & highlights
No Placebo-Only Group

Summary

This trial is testing if FibroScan, a device that uses sound waves to check for liver damage, is safe for patients with chronic liver disease who have pacemakers or ICDs. The study aims to ensure that using FibroScan does not interfere with these implanted heart devices. FibroScan is a non-invasive device that uses sound waves to measure liver stiffness and has been shown to be reliable for assessing liver fibrosis and cirrhosis.

Eligible Conditions
  • Non-invasive Indices to Predict Hepatic Fibrosis in BA Patients.
  • Liver Cirrhosis

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~up to 5 years
This trial's timeline: 3 weeks for screening, Varies for treatment, and up to 5 years for reporting.

Treatment Details

Awards & Highlights

No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.

Trial Design

1Treatment groups
Experimental Treatment
Group I: FibroscanExperimental Treatment1 Intervention
Fibroscan under simultaneous cardiac monitoring
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Fibroscan
2016
N/A
~1140

Find a Location

Who is running the clinical trial?

University of SaskatchewanLead Sponsor
256 Previous Clinical Trials
154,252 Total Patients Enrolled
Lawrence Worobetz, MDPrincipal InvestigatorUniversity of Saskatchewan
~19 spots leftby Nov 2025
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