Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
400 participants
OBSERVATIONAL
2024-09-01
2028-09-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Patients with polycythemia
Whatever the origin of polycythemia
Collection of tube bottoms from blood samples taken in the clinic
Collection of tube bottoms from blood samples taken in the clinic
Patient controls
Patients with the same pathological features but without polycythemia
Collection of tube bottoms from blood samples taken in the clinic
Collection of tube bottoms from blood samples taken in the clinic
Interventions
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Collection of tube bottoms from blood samples taken in the clinic
Collection of tube bottoms from blood samples taken in the clinic
Eligibility Criteria
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Inclusion Criteria
Patients with polycythemia:
* haemoglobin value \> 16 g/dl female or \> 16.5 g/dl male
* with a well-identified cause: either primary (polycythemia Vaquez, erythropoietin receptor or LNK/SH2B3 mutation...) or secondary \[cardio-respiratory pathologies, renal pathologies (post-transplant, polycystic kidney disease), metabolic pathologies, tumour (leiomyoma, pheochromocytoma...), constitutional mutations (hyperaffine haemoglobins, HIF2/EPAS1, PHD/EGLN1, VHL, ...)
Patients control:
\- persons with a similar pathology to that of polycythemia patients, essentialy secondary, but without polycythemia, i.e. with a haemoglobin value of \< 16 g/DL for women and \< 16.5 g/DL for men
Exclusion Criteria
* Person subject to a court order
* Pregnant, parturient or nursing woman
* Incapable of expressing consent
* Minor
18 Years
ALL
No
Sponsors
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Centre Hospitalier Universitaire Dijon
OTHER
Responsible Party
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Locations
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CHU Dijon Bourgogne
Dijon, , France
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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GIRODON_2024
Identifier Type: -
Identifier Source: org_study_id
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