Survey Evaluating the Psychosocial Effects of Living With Haemophilia
NCT01322620 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 1236
Last updated 2017-02-23
Summary
This study is conducted in Africa, Asia, Europe, North America and South America.
The purpose of the survey is to identify the key psychosocial issues affecting patients with haemophilia.
Conditions
- Congenital Bleeding Disorder
- Haemophilia A
- Haemophilia B
- Haemophilia A With Inhibitors
- Haemophilia B With Inhibitors
- Relatives to/Carers of Patients
Interventions
- OTHER
-
No treatment given
No treatment given. Participants are to complete a questionnarie in the study.
Sponsors & Collaborators
- lead INDUSTRY
Principal Investigators
-
Global Clinical Registry (GCR, 1452) · Novo Nordisk A/S
Eligibility
- Min Age
- 18 Years
- Sex
- MALE
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2011-06-03
- Primary Completion
- 2012-02-29
- Completion
- 2012-02-29
Countries
- Canada
- Spain
- United Kingdom
Study Locations
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