CClinicalTrials.gg
CompletedNCT00798499Updated Jul 2, 2009

A Feasibility Study to Collect Data in Patients With Haemophilia

An observational study in Hemophilia, sponsored by AstraZeneca. Completed at 2 sites in Sweden. Open to male participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2009-07-02.

Sponsored by AstraZeneca · Observational

Study type
Observational
Model
Case-only
Enrollment
50
Ages
18 Years and older
Sex
Male
01

Study 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.

02

Conditions studied

  • Hemophilia

Browse trials for

Keywords

  • haemophilia
  • patients with haemophilia
03

In context

Hemophilia A

866 studies on the registry are indexed under Hemophilia A; 137 are open to participants now.

This study's planned enrollment of 50 is below the median of 80 across 314 observational studies indexed under Hemophilia A.

Browse Hemophilia A studies →

Lead sponsor

AstraZeneca is the lead sponsor of 3,429 studies on the registry; 270 are open to participants now.

Of its 357 completed or terminated interventional studies of FDA-regulated products, 173 (48%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
Male
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Patients with haemophilia

Inclusion criteria

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

Exclusion criteria

Exclusion Criteria:

  • No exclusion criteria
05

Study design

Observational model
Case-only
Enrollment
50 participants (estimated)
Biospecimen retention
Samples without dna

Groups and cohorts

  • 1

    Laboratory variables

    Other: Laboratory variables

Interventions

  • OtherLaboratory variables

    1 visit

06

What researchers measure

Primary outcomes

  1. Laboratory variables related to coagulation, SAEs in connection to blood sampling procedures will be collected, non-serious AEs will not be recorded

    Time frame: The variables will be measured at first visit.

07

Study locations

2 sites
  • Research Site
    Malmö, Sweden
  • Research Site
    Stockholm, Sweden
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 2, 2009, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT00798499
Lead sponsor
AstraZeneca
First posted
Nov 26, 2008
Start date
Dec 2008
Completion
Jun 2009
Last update
Jul 2, 2009

Study contacts

Erik Berntorp, MD, PhD, Professor
principal investigator · Malmo University
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jul 2009. You cannot join it, but the record below documents what was studied.

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