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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05009537
Other study ID # CARTOGEN - 29BRC21.0211
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date September 2021
Est. completion date September 2026

Study information

Verified date August 2021
Source University Hospital, Brest
Contact Marie-Bérengère, TROADEC, PhD
Phone (33)230338055
Email Marie-berengere.troadec@chu-brest.fr
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Establish the diagnostic potential of optical genome mapping in patients with suspected hematologic cancer


Recruitment information / eligibility

Status Recruiting
Enrollment 200
Est. completion date September 2026
Est. primary completion date September 2022
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility 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


Related Conditions & MeSH terms


Locations

Country Name City State
France CHRU de Brest Brest
France CH Morlaix, service d'hémato clinique Morlaix
France CHIC, service d'hémato clinique Quimper
France CH St Brieuc, service d'hémato clinique Saint-Brieuc

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Brest

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Establish the diagnostic potential of optical genome mapping in patients with suspected hematologic cancer identification of anomalies by mapping identical to those identified by combining conventional cytogenetics and FISH. 2021-2026
Secondary identification of new chromosomal abnormalities of clinical relevance. 2021-2026
Secondary identification of new chromosomal anomalies involved in oncogenic pathways 2021-2026
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