Genetic Markers and Biomarkers in Patients With Intellectual Disabilities of Genetic Origin
- Sponsor
- Institut Jerome Lejeune
- Study ID
- NCT05767203
- Status
- Recruiting
Conditions
- Down Syndrome
- Intellectual Disability
Eligibility Criteria
- Sex
- ALL
- Age
- N/A - N/A
- Healthy Volunteers
- Accepted
Interventions
- Biological samplings — OTHERBlood and/or skin samples
Study Details
Analyze genetic and biological markers in patients with Intellectual Deficiencies (ID) of genetic origin in order to better understand the mechanisms of modified genes, cellular mechanisms, pathways involved in different disorders , complications and pathologies associated with ID of genetic origin.
Key Dates
- First listed
- Mar 14, 2023
- Start date
- Sep 1, 2022
- Status verified
- Mar 2023
- Primary completion
- Sep 1, 2032
- Completion
- Dec 31, 2032
Study Design
- Enrollment
- 2,000 participants (estimated)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- BASIC_SCIENCE
Arms
- Experimental: Patients with Down syndrome or other Intellectual deficiency of genetic originPatients with Down syndrome or with other intellectual deficiency of genetic origin followed at the outpatients clinic of the Institut Jérôme Lejeune.
Primary Outcome Measure
Identification of biomarkers in blood [ Time Frame: 10 years ]
Central Contacts
- Sophie Durand+33156586300
Related Studies
- Specimen Collection from Pregnant Women At Increased Risk for Fetal AneuploidyRecruiting · Sequenom, Inc. · Birmingham, Alabama
- Computer Models of Airways in Children and Young Adults With Sleep Apnea and Down SyndromeEnrolling By Invitation · Children's Hospital Medical Center, Cincinnati · Cincinnati, Ohio
- DS-Connect®: The Down Syndrome RegistryRecruiting · University of Colorado, Denver · Aurora, Colorado
- The Human Trisome ProjectRecruiting · University of Colorado, Denver · Denver, Colorado