Actively Recruiting

MALE
NCT06574984

Study for Turoctocog Alfa Treatment Regimen in Iraqi Haemophilia A Patients

Led by Novo Nordisk A/S · Updated on 2026-02-13

900

Participants Needed

7

Research Sites

76 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The study has descriptive purposes, with aim of assessing how turoctocog alfa is used in the everyday practice and to provide a baseline for the management of haemophilia A and does not involve any change in the clinical management of participants. Data will be extrapolated from the existing paper based medical records and uploaded to an electronic database specifically created for the study. Baseline information/history will be recorded at time of switching from previous FVIII replacement therapy to turoctocog alfa from the enrolled participants and outcomes will be collected according to participants visit format.

CONDITIONS

Official Title

Study for Turoctocog Alfa Treatment Regimen in Iraqi Haemophilia A Patients

Who Can Participate

MALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Male patients, both children and adults
  • Patients diagnosed with haemophilia A of any severity
  • Patients treated on-demand or with prophylaxis
  • Patients previously treated with factor VIII replacement therapy
Not Eligible

You will not qualify if you...

  • Patients with coagulation disorders other than haemophilia A, such as Von Willebrand disease
  • Patients with documented presence of any factor VIII inhibitor

AI-Screening

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Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 7 locations

1

National centre for Hamophilia

Baghdad, Iraq, 10001

Enrolling by Invitation

2

Novo Nordisk Investigational Site

Baghdad, Iraq

Actively Recruiting

3

Basrah Haemoplhilia centre

Basra, Iraq, 61001

Not Yet Recruiting

4

Hilla Haemophilia centre

Hillah, Iraq, 51001

Enrolling by Invitation

5

Karbala Haemophilia centre

Karbala, Iraq, 56001

Enrolling by Invitation

6

Kirkuk Centre for Cancer and Blood Disorders

Kirkuk, Iraq, 36001

Enrolling by Invitation

7

Najaf Haemophilia Centre

Najaf, Iraq, 54001

Enrolling by Invitation

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Research Team

N

Novo Nordisk

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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