Brief Title
A Feasibility Study to Collect Data in Patients With Haemophilia
Official Title
A Multi Centre Study With no Treatment, Designed to Gain Information About the Haemophilia Patient Population
Brief Summary
The purpose of this study is to collect reference data in patients with haemophilia. The study will also collect and store blood samples for potential future exploratory research in the disease area.
Study Type
Observational
Primary Outcome
Laboratory variables related to coagulation, SAEs in connection to blood sampling procedures will be collected, non-serious AEs will not be recorded
Condition
Hemophilia
Intervention
Laboratory variables
Study Arms / Comparison Groups
1
Description: Laboratory variables
Publications
* Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline.
Recruitment Information
Recruitment Status
Other
Estimated Enrollment
50
Start Date
December 2008
Completion Date
June 2009
Eligibility Criteria
Inclusion Criteria: - Provision of written informed consent - Patients with haemophilia, all severities - At least 18 years old. Exclusion Criteria: - No exclusion criteria
Gender
Male
Ages
18 Years - N/A
Accepts Healthy Volunteers
No
Contacts
Erik Berntorp, MD, PhD, Professor, ,
Location Countries
Sweden
Location Countries
Sweden
Administrative Informations
NCT ID
NCT00798499
Organization ID
D0960M00006
Study Sponsor
AstraZeneca
Study Sponsor
Erik Berntorp, MD, PhD, Professor, Principal Investigator, Malmo University
Verification Date
July 2009