Joint Disease Clinical Trial
— KAPPAOfficial title:
Key Aspects of Medical Practice in Patients With Haemophilia A
NCT number | NCT02996942 |
Other study ID # | 2012/118 |
Secondary ID | |
Status | Withdrawn |
Phase | |
First received | |
Last updated | |
Start date | July 2012 |
Est. completion date | December 2017 |
Verified date | December 2018 |
Source | Lund University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational [Patient Registry] |
The KAPPa project has the aim to create an international database in which information about clinical features, therapeutic management, burden of illness and costs of severe and moderate haemophilia A patients from different countries and sites is collected. The aim of this project is to analyse the influence of such different characteristics on medical, psychosocial and economic outcomes in patients over the long-term.
Status | Withdrawn |
Enrollment | 0 |
Est. completion date | December 2017 |
Est. primary completion date | December 2017 |
Accepts healthy volunteers | No |
Gender | All |
Age group | N/A and older |
Eligibility |
Inclusion Criteria: or forms. - severe haemophilia A (factor VIII<1%) - moderate (factor VIII<5%) - signed informed consent Exclusion Criteria: - Not fullfilling inclusion criteria |
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
Lund University |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Outcome of factor replacement treatment | Joint disase according to HJHS. Quality of Life. Health economic evalaution. | 3 years |
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