Optical Genome Mapping in Hematological Malignancies

NCT ID: NCT05009537

Last Updated: 2021-08-17

Study Results

Results pending

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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Recruitment Status

RECRUITING

Total Enrollment

200 participants

Study Classification

OBSERVATIONAL

Study Start Date

2021-09-30

Study Completion Date

2026-09-30

Brief Summary

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

Detailed Description

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Conditions

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MDS ALL Other Hematologic Malignant Neoplasms

Study Design

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Observational Model Type

COHORT

Study Time Perspective

RETROSPECTIVE

Eligibility Criteria

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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
Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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University Hospital, Brest

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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CHRU de Brest

Brest, , France

Site Status RECRUITING

CH Morlaix, service d'hémato clinique

Morlaix, , France

Site Status RECRUITING

CHIC, service d'hémato clinique

Quimper, , France

Site Status RECRUITING

CH St Brieuc, service d'hémato clinique

Saint-Brieuc, , France

Site Status RECRUITING

Countries

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France

Central Contacts

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Marie-Bérengère, TROADEC, PhD

Role: CONTACT

(33)230338055

Nathalie DOUET-GUILBERT, MD, PhD

Role: CONTACT

(33)230338055

Facility Contacts

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Marie-Bérengère, TROADEC

Role: primary

Christophe NICOL, MD

Role: primary

Léanig LE CLEACH, MD

Role: primary

Cédric DUCLOS, MD

Role: primary

Other Identifiers

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CARTOGEN - 29BRC21.0211

Identifier Type: -

Identifier Source: org_study_id

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