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Fibroscan for Liver Cirrhosis
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 30 min
Awards & highlights
Study Summary
This study is designed to determine if the Fibroscan (Echosens, Paris), a non-invasive, ultrasound-based device used to estimate fibrosis in patients with chronic liver disease, interferes with implanted cardiac pacemaker and/or implantable cardioverter-defibrillators. Recruitment consists of a total of 200 outpatients undergoing routine pacemaker interrogation at a teaching-hospital pacemaker clinic.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowTimeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 30 min
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~30 min
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Rate of Pacemaker/ICD malfunction
Type of Pacemaker/ICD malfunction
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
~1100
Find a Location
Who is running the clinical trial?
University of SaskatchewanLead Sponsor
251 Previous Clinical Trials
154,210 Total Patients Enrolled
Lawrence Worobetz, MDPrincipal InvestigatorUniversity of Saskatchewan
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