Brief Title
Health Related Quality of Life of Youth and Young Adults With Hemophilia A
Official Title
A Prospective Non-Interventional Study to Describe Health Related Quality of Life of Youth and Young Adults With Moderate or Severe Hemophilia A Using Recombinant Factor VIII (Helixate FS).
Brief Summary
The relevance of the study will be in establishing whether Health Related Quality of Life (HRQoL) measures obtained repeatedly during hemophilia care are sensitive to significant changes in health or personal circumstances related to the transition from youth to adulthood. This may support the future use of HRQoL measures as part of routine care in order to identify important changes that are not detectible by other clinical means.
Study Type
Observational
Primary Outcome
Health Related Quality of Life (HRQoL)
Secondary Outcome
Sensitivity of HRQoL measures to significant life events
Condition
Hemophilia A
Study Arms / Comparison Groups
Patients
Description: Patients who have moderate or severe Hemophilia A, living in Canada and who are using Helixate FS either on-demand or prophylaxis
Publications
* Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline.
Recruitment Information
Estimated Enrollment
48
Start Date
October 2009
Completion Date
November 2013
Primary Completion Date
July 2013
Eligibility Criteria
Inclusion Criteria: - Moderate or severe Hemophilia A (factor level ≤5%) - Receiving Helixate FS as on-demand treatment or prophylaxis therapy at time of informed consent - Patient age 14 to 29 years at the time of recruitment - Complete informed consent process and documentation; (Patients under age 18 must assent in addition to consent of legal guardian) - Willing/able to follow study protocol, including keeping a bleeding and treatment diary - Able to communicate clearly in either English or French - both written and verbal communication is essential. Exclusion Criteria: - Known inhibitor at time of recruitment (> 0,5 Bethesda units) or immune tolerance therapy at time of recruitment - HIV positive - Symptomatic Hepatitis B or C infection or active treatment for hepatitis B or C - Inability to comply with study protocol - Hypersensitivity to Helixate FS or to any ingredients in the formulation or component of the container - Hypersensitivity to mouse or hamster protein - Unsuitable to participate in study for any other reason as assessed by investigator
Gender
Male
Ages
14 Years - 30 Years
Accepts Healthy Volunteers
No
Contacts
Jean St-Louis, MD, ,
Location Countries
Canada
Location Countries
Canada
Administrative Informations
NCT ID
NCT01034904
Organization ID
CE1250_5002_CA
Responsible Party
Sponsor
Study Sponsor
CSL Behring
Study Sponsor
Jean St-Louis, MD, Principal Investigator, St. Justine's Hospital
Verification Date
December 2013