Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
Register:
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ClinicalTrials.gov |
Last refreshed on:
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23 May 2016 |
Main ID: |
NCT02415348 |
Date of registration:
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08/04/2015 |
Prospective Registration:
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No |
Primary sponsor: |
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Public title:
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The Use of Fibroscan to Assess Liver Fibrosis in Patients With Cardiac Pacemakers
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Scientific title:
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The Use of Fibroscan to Assess Liver Fibrosis in Patients With Cardiac Pacemakers and/or Implantable Cardioverter-Defibrillators |
Date of first enrolment:
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April 2015 |
Target sample size:
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200 |
Recruitment status: |
Active, not recruiting |
URL:
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https://clinicaltrials.gov/show/NCT02415348 |
Study type:
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Interventional |
Study design:
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Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Diagnostic
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Phase:
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N/A
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Countries of recruitment
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Canada
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Contacts
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Name:
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Lawrence Worobetz, MD |
Address:
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Telephone:
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Email:
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Affiliation:
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University of Saskatchewan |
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Key inclusion & exclusion criteria
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Inclusion Criteria:
-Any outpatient undergoing routine pacemaker interrogation at pacemaker clinic
Exclusion Criteria:
- Pregnancy
- BMI>35
- Person with active implantable medical devices other than cardiac pacemaker and/or
ICD
- Person who are unable to tolerate lying flat for the FibroScan examination.
Age minimum:
16 Years
Age maximum:
N/A
Gender:
Both
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Health Condition(s) or Problem(s) studied
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Liver Cirrhosis
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Intervention(s)
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Device: Fibroscan
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Primary Outcome(s)
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Type of Pacemaker/ICD malfunction
[Time Frame: 30 min]
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Rate of Pacemaker/ICD malfunction
[Time Frame: 30 min]
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Secondary ID(s)
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Bio 15-35
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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