Retrospective Study in Chinese Pediatric Hemophilia A Patients With rFⅧ Contained Regular Prophylaxis
NCT02263066 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 181
Last updated 2015-07-17
Summary
To assess and describe real-life treatment choices for rFⅧ contained regular prophylaxis/bleeding prevention treatment in pediatric hemophilia patients in China (2007-2013)
Conditions
Interventions
- BIOLOGICAL
-
BAY14-2222_Kogenate-FS FVIII
Depends on Doctor's decision
Sponsors & Collaborators
- lead INDUSTRY
Principal Investigators
-
Bayer Study Director · Bayer
Eligibility
- Min Age
- 2 Years
- Max Age
- 18 Years
- Sex
- MALE
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2014-10-31
- Primary Completion
- 2015-07-31
- Completion
- 2015-07-31
Countries
- China
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