A Feasibility Study to Collect Data in Patients With Haemophilia

A Multi Centre Study With no Treatment, Designed to Gain Information About the Haemophilia Patient Population

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT00798499

Enrollment

Registered

2008-11-26

Start date

2008-12-31

Completion date

2009-06-30

Last updated

2009-07-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hemophilia

Keywords

haemophilia, patients with haemophilia

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.

Interventions

OTHERLaboratory variables

1 visit

Study design

Observational model

CASE_ONLY

Eligibility

Sex/Gender

MALE

Age

18 Years to No maximum

Healthy volunteers

Inclusion criteria

* Provision of written informed consent * Patients with haemophilia, all severities * At least 18 years old.

Exclusion criteria

* No

Design outcomes

Primary

Measure	Time frame
Laboratory variables related to coagulation, SAEs in connection to blood sampling procedures will be collected, non-serious AEs will not be recorded	The variables will be measured at first visit.

Countries

Sweden

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026