Optical Genome Mapping in Hematological Malignancies
Recruiting
- Conditions
- ALLMDSOther Hematologic Malignant Neoplasms
- Registration Number
- NCT05009537
- Lead Sponsor
- University Hospital, Brest
- Brief Summary
Establish the diagnostic potential of optical genome mapping in patients with suspected hematologic cancer
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- All
- Target Recruitment
- 200
Inclusion Criteria
- Minor/Major Patients
- Patients with suspected hemopathies for whom we receive a sample for diagnosis in the chromosomal genetics laboratory or for whom a diagnosis of hemopathy has already been made.
- No objection made or consent given
Exclusion Criteria
- Patients under judicial protection (guardianship, curatorship, ...),
- Refusal to participate
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Establish the diagnostic potential of optical genome mapping in patients with suspected hematologic cancer 2021-2026 identification of anomalies by mapping identical to those identified by combining conventional cytogenetics and FISH.
- Secondary Outcome Measures
Name Time Method identification of new chromosomal abnormalities of clinical relevance. 2021-2026 identification of new chromosomal anomalies involved in oncogenic pathways 2021-2026
Trial Locations
- Locations (4)
CHIC, service d'hémato clinique
🇫🇷Quimper, France
CHRU de Brest
🇫🇷Brest, France
CH Morlaix, service d'hémato clinique
🇫🇷Morlaix, France
CH St Brieuc, service d'hémato clinique
🇫🇷Saint-Brieuc, France