Trials / Completed
CompletedNCT01322620
Survey Evaluating the Psychosocial Effects of Living With Haemophilia
Haemophilia, Experiences, Results and Opportunities (HERO): A Community-based Evaluation of the Psychosocial Effects of Haemophilia on Patients and Their Carers
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 1,236 (actual)
- Sponsor
- Novo Nordisk A/S · Industry
- Sex
- Male
- Age
- 18 Years
- Healthy volunteers
- Not accepted
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
| Type | Name | Description |
|---|---|---|
| OTHER | No treatment given | No treatment given. Participants are to complete a questionnarie in the study. |
Timeline
- Start date
- 2011-06-03
- Primary completion
- 2012-02-29
- Completion
- 2012-02-29
- First posted
- 2011-03-24
- Last updated
- 2017-02-23
Locations
3 sites across 3 countries: Canada, Spain, United Kingdom
Source: ClinicalTrials.gov record NCT01322620. Inclusion in this directory is not an endorsement.