Real-World use of clotting factor in iraqi haemophilia patients examined

NCT ID NCT06574984

First seen Nov 01, 2025 · Last updated Jun 23, 2026 · Updated 26 times

Summary

This completed study observed how 329 Iraqi male patients with haemophilia A used turoctocog alfa (a clotting factor) in their daily care. Researchers reviewed medical records to see how the drug was given and how many bleeding episodes occurred. The goal was to describe real-world treatment patterns, not to change how patients were treated.

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This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.

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Contacts and locations

Locations

  • Basrah Haemoplhilia centre

    Basra, 61001, Iraq

  • Hilla Haemophilia centre

    Hillah, 51001, Iraq

  • Karbala Haemophilia centre

    Karbala, 56001, Iraq

  • Kirkuk Centre for Cancer and Blood Disorders

    Kirkuk, 36001, Iraq

  • Najaf Haemophilia Centre

    Najaf, 54001, Iraq

  • National centre for Hamophilia

    Baghdad, 10001, Iraq

  • Novo Nordisk Investigational Site

    Baghdad, Iraq

What this could mean

Our plain-language read of the trial. This is informational only — not medical advice or a prediction.

Active substance

turoctocog alfa (a clotting factor VIII replacement therapy)

What this could lead to

If successful, this study could help doctors understand how turoctocog alfa is used in real-world settings and guide better management of haemophilia A.

What could go wrong

This is an observational study that only looks back at existing records, so it cannot prove cause and effect. Results may not apply to other populations or settings.

Conditions

The condition(s) this trial relates to.

hemophilia A

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.