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Elastography of the Liver in Cystic Fibrosis Patients. Diagnostic and Prognostic Aspects

Primary Purpose

Cystic Fibrosis, Liver Fibrosis

Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Fibroscan
Sponsored by
Karolinska University Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Cystic Fibrosis focused on measuring cystic fibrosis, elastography, liver biopsy

Eligibility Criteria

1 Year - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Verified cystic fibrosis

Exclusion Criteria:

Sites / Locations

    Arms of the Study

    Arm 1

    Arm Type

    Other

    Arm Label

    Elastography

    Arm Description

    Fibroscan elastography device for evaluation of liver disease in CF patients.

    Outcomes

    Primary Outcome Measures

    Elastographic Value in kPa Measured by Fibroscan
    Elastographic values given in kPa by Fibroscan. All patients undergo elastographic measurement of the liver and ultrasound of the liver. The grade of fibrosis is to be established by setting the cut-off for cystic fibrosis patients.

    Secondary Outcome Measures

    Full Information

    First Posted
    May 4, 2015
    Last Updated
    November 1, 2016
    Sponsor
    Karolinska University Hospital
    Collaborators
    Karolinska Institutet
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    1. Study Identification

    Unique Protocol Identification Number
    NCT02603666
    Brief Title
    Elastography of the Liver in Cystic Fibrosis Patients. Diagnostic and Prognostic Aspects
    Official Title
    Elastography of the Liver in Cystic Fibrosis Patients. Diagnostic and Prognostic Aspects
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    November 2016
    Overall Recruitment Status
    Completed
    Study Start Date
    January 2012 (undefined)
    Primary Completion Date
    June 2014 (Actual)
    Study Completion Date
    June 2014 (Actual)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Karolinska University Hospital
    Collaborators
    Karolinska Institutet

    4. Oversight

    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    The aim of the study is to find CF patients at risk for cystic fibrosis related liver disease (CFLD). Comparison of ultrasound by two modalities and biochemical markers with histological evaluation of liver biopsy if present.
    Detailed Description
    There are 209 CF patients attending Stockholm Cystic Fibrosis Center (January 2010). All up till 15 years of age are screened for liver disease annually by ultrasound (US) and also by biochemical markers. Ultrasound is performed every third year over 15 years of age in patients without CFLD, while all of them with diagnosed CFLD are continued to be investigated annually. Biochemical markers are controlled at least once every year in all CF patients. Elastography of the liver will be planned together with the investigations of the annual follow up, in an optimal clinical status. If either US or elastography of the liver indicates liver disease or progress of the already existing pathological changes, a liver biopsy will be performed according to routine procedure at Stockholm CF Centre. Also, historical data of liver biopsies and biochemical investigations will be considered in the study. Elastography of the liver will be performed by Fibroscan device, with transducers for children and adults, respectively. Clinical importance Liver US investigations in CF patients have important implications but are difficult to standardize in a routine clinical setting. Elastography may have an advantage in the evaluation of early fibrosis with clinical importance in pursuing diagnostics and intensifying treatment. A significant group (up to 25 %) of CF patients may be helped by this novel method. Including histological data, accuracy of elastography in CF patients may be improved. Further details of the importance of fatty acid status in CF may be elucidated.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Cystic Fibrosis, Liver Fibrosis
    Keywords
    cystic fibrosis, elastography, liver biopsy

    7. Study Design

    Primary Purpose
    Diagnostic
    Study Phase
    Not Applicable
    Interventional Study Model
    Single Group Assignment
    Masking
    None (Open Label)
    Allocation
    N/A
    Enrollment
    130 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    Elastography
    Arm Type
    Other
    Arm Description
    Fibroscan elastography device for evaluation of liver disease in CF patients.
    Intervention Type
    Device
    Intervention Name(s)
    Fibroscan
    Other Intervention Name(s)
    Elastography
    Intervention Description
    Ultrasound by specific wavelength developed for elastography, repeated measures according to the manufacturer's instructions.
    Primary Outcome Measure Information:
    Title
    Elastographic Value in kPa Measured by Fibroscan
    Description
    Elastographic values given in kPa by Fibroscan. All patients undergo elastographic measurement of the liver and ultrasound of the liver. The grade of fibrosis is to be established by setting the cut-off for cystic fibrosis patients.
    Time Frame
    Within 28 days in connection with their annual evaluation at a single point of time

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    1 Year
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Verified cystic fibrosis Exclusion Criteria:
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Ferenc Karpati, MD, PhD
    Organizational Affiliation
    Stockholm CF Center, Karolinska University Hospital
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Plan to Share IPD
    Yes

    Learn more about this trial

    Elastography of the Liver in Cystic Fibrosis Patients. Diagnostic and Prognostic Aspects

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