Clinical Trials in France / NCT05626465
Starting soon
Observational
Biomarker-s of Abusive Head Trauma by Proteomics
NCT05626465 · tracked via the Priya Life Science France tracker
Condition(s) studied
Abuse, ChildProtein Disorder, Blood
Investigational drug(s) / intervention(s)
Blood test
Blood test: Proteomic analyses on serum
Study summary
The aim of our study is to highlight biomarker-s of Abusive Head Trauma by proteomics analyses on the serum of child victims of abuse.
Eligibility
Inclusion Criteria:
* Age : 0-2 y.o
* Medical consultation for malaise, seizure (without fever), loss of consciousness, traumatic bain injury, or cranioplasty
* Blood test during medical care
* Accepted informed consent
Exclusion Criteria:
* Refused informed consent
* For control groups : medical history of child abuse
* For AHT group : rare metabolic disease (Menkes, etc..)
Primary outcome measure(s)
- Highlight novel biomarker-s of AHT — Hospital admission to discharge (up to 3 days)
Proteomic analyses will be made on serum of infant victim of AHT. Results will be compare with control groups (traumatic brain injury, cranioplasty, malaise).
Trial sites (2)
| Facility | City | Region | Status |
|---|---|---|---|
| Ginhoux Thiphanie | Lyon | Rhône | |
| Wiskott Kim | Geneva | Switzerland |
More University Hospital, Geneva trials in France
Official registry record
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT05626465 on ClinicalTrials.gov ↗ ← All trials in France