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Optical Genome Mapping in Hematological Malignancies

Recruiting
Conditions
ALL
MDS
Other 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
NameTimeMethod
Establish the diagnostic potential of optical genome mapping in patients with suspected hematologic cancer2021-2026

identification of anomalies by mapping identical to those identified by combining conventional cytogenetics and FISH.

Secondary Outcome Measures
NameTimeMethod
identification of new chromosomal abnormalities of clinical relevance.2021-2026
identification of new chromosomal anomalies involved in oncogenic pathways2021-2026

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

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