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German Pediatric Hemophilia Research Database

German Pediatric Hemophilia Research Database

Not Recruiting
18 years and younger
All
Phase N/A
  • Technical (Original)
  • Simplified (AI rewritten)

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Overview

The German Pediatric Hemophilia Research Database will collect data on the prophylactic and therapeutic use of factor concentrates, complications, outcome measures (joint scores, QoL) and living circumstances in newly diagnosed children with hemophilia.

Eligibility

Inclusion Criteria:

  • hemophilia A or B
  • FVIII/FIX \<1% to 25%
  • informed consent

Exclusion Criteria:

  • no consent

Study details
    Hemophilia A
    Hemophilia B
    Children
    Drug Specific Antibodies

NCT02912143

Goethe University

10 October 2026

Contact a study center

FAQs

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A clinical trial is a study designed to test specific interventions or treatments' effectiveness and safety, paving the way for new, innovative healthcare solutions.

Why should I take part in a clinical trial?

Participating in a clinical trial provides early access to potentially effective treatments and directly contributes to the healthcare advancements that benefit us all.

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The duration of clinical trials varies. Some trials last weeks, some years, depending on the phase and intention of the trial.

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