Bridging Hemophilia B Experiences, Results and Opportunities Into Solutions (B-HERO-S)
NCT ID: NCT02568202
Last Updated: 2016-01-12
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
449 participants
OBSERVATIONAL
2015-09-30
2015-11-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Survey
No treatment given
This is an online web-based cross-sectional survey in which participants will complete one of two questionnaires.
There will be no treatment.
Interventions
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No treatment given
This is an online web-based cross-sectional survey in which participants will complete one of two questionnaires.
There will be no treatment.
Eligibility Criteria
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Inclusion Criteria
* Caregivers of children currently aged below 18 years with hemophilia B (any severity, with or without inhibitors)
* Subjects must have access to the internet, either at home or at a location convenient to them
* Provision of informed consent before the start of any survey-related activities
Exclusion Criteria
* Previous completion of the B-HERO-S study with receipt of compensation
* Mental incapacity, unwillingness or language barriers precluding adequate understanding or cooperation
18 Years
ALL
No
Sponsors
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Novo Nordisk A/S
INDUSTRY
Responsible Party
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Principal Investigators
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Global Clinical Registry (GCR, 1452)
Role: STUDY_DIRECTOR
Novo Nordisk A/S
Locations
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Novo Nordisk Clinical Trial Call Center
Plainsboro, New Jersey, United States
Countries
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Related Links
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Clinical Trials at Novo Nordisk
Other Identifiers
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U1111-1171-8168
Identifier Type: OTHER
Identifier Source: secondary_id
HAEM-4268
Identifier Type: -
Identifier Source: org_study_id
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