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NCT Number: NCT02912143

German Pediatric Hemophilia Research Database

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.

Recruiting

Interested in participating?

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Key information

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

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

Exclusion criteria

  • no consent

Treatment and study plan

documentation only

Other

Primary outcomes

  1. Number of patients with antibody developement to exogenous clotting factors (>0.5 BU)

    Time frame: 5 years

    Blood Test: measurement in Bethesda Units, positive according to local standards, for most labs > 0.5 BU

Interested in participating?

Recruiting

Interested in participating?

Request Info

Sponsors and collaborators

Lead sponsor

Goethe University

Other

Collaborators

  • Society for Thrombosis and Haemostasis Research (Germany)

Registry information

Acronym: GEPHARD

Important dates

Study start
2017
Primary completion
2027
Study completion
2028
First posted
Sep 23, 2016
Registry last updated
Mar 8, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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