Last updated: January 16, 2024
Sponsor: University Hospital, Bordeaux
Overall Status: Active - Recruiting
Phase
N/A
Condition
N/ATreatment
Histone acetylation profiles of cells of SRT patients with CREBBP mutations
Culture of lymphoblastoid line from blood sample
Generation of Induced Pluripotent Stem Cells (iPSC) from fibroblasts obtained by skin biopsy
Clinical Study ID
NCT04122742
CHUBX 2019/19
Ages > 2 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
- Patient with a clinical and molecular diagnosis of RSTS
- Patients carrying the CREBBP or EP300 variants
- Patients older than 2 years
- Affiliated patients or beneficiaries of a social security scheme.
- Free, informed and signed consent by the parents or holder of parental authority forminor patients
- Free, informed and signed consent by the patient representative for the major patientsunder guardianship
- Free, informed and signed consent by the patient for major patients
Exclusion
Exclusion Criteria: Patients having:
- a history of allergy to any product or device that may be used before, during, andafter the biopsy;
- cutaneous disease of the areas where the biopsy is to be performed
- underwent physical treatment (radiotherapy, ...) on the area to be biopsied, duringthe last 6 months
- hereditary or acquired disorders of hemostasis Patients under treatment:
- likely to act on the haemostasis (anticoagulants, platelet antiaggregants, ...) in themonth preceding the inclusion and during the study
- by histone deacetylase inhibitor (sodium valproate) likely to interfere with theinterpretation of the results.
Study Design
Total Participants: 154
Treatment Group(s): 5
Primary Treatment: Histone acetylation profiles of cells of SRT patients with CREBBP mutations
Phase:
Study Start date:
October 08, 2019
Estimated Completion Date:
October 31, 2025
Study Description
Connect with a study center
Centre Hospitalier Universitaire de Bordeaux
Talence, 33400
FranceActive - Recruiting
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