Trials / Unknown
UnknownNCT03263364
Genomic Screening for Hereditary Erythrocytosis and Related Diseases
- Status
- Unknown
- Phase
- —
- Study type
- Observational
- Enrollment
- 150 (estimated)
- Sponsor
- Centre Hospitalier Universitaire Dijon · Academic / Other
- Sex
- All
- Age
- —
- Healthy volunteers
- Not accepted
Summary
Unexplained polycythemias are rare diseases, and therefore, the collection of data inherent to these diseases will not only improve their characterisation, but also allow stratification according to the risks and the course of the disease. The objective of this project is to constitute a database on the disease which will allow us to better understand it and in due course improve its management. The GENRED project thus bears uniquely on the collection of information, which will be gathered throughout the usual management of patients for this type of disease.
Conditions
Timeline
- Start date
- 2016-10-01
- Primary completion
- 2020-10-01
- Completion
- 2020-10-01
- First posted
- 2017-08-28
- Last updated
- 2017-08-28
Locations
2 sites across 1 country: France
Source: ClinicalTrials.gov record NCT03263364. Inclusion in this directory is not an endorsement.