Glial Fibrillary Acidic Protein (GFAP) and Ubiquitin Carboxy-terminal Hydrolase L1 (UCH-L1) to Exclude Lesions Linked to Significant Traumatic Brain Injuries

NCT05885529 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 1500

Last updated 2025-02-19

No results posted yet for this study

Summary

The goal of this observational study is to evaluate the performance of UCH-L1 and GFAP combined in patients with a mild traumatic brain injury. The main question :

• Does the combination of UCH-L1 and GFAP can exclude brain injuries detected with CT scan in the first twelve hours after a mild traumatic brain injury?

Participants will do the exams planed in routine care and :

* during the expected blood sampling an additional blood sample will be done,
* seven days after the discharge a call will be done by the investigator.

Conditions

Interventions

OTHER

UCH-L1 GFAP

measurment of UCH-L1 GFAP within 12 hours in adult patients after a mild traumatic brain injury

Sponsors & Collaborators

  • BioMérieux

    collaborator INDUSTRY
  • Assistance Publique - Hôpitaux de Paris

    collaborator OTHER
  • University Hospital, Clermont-Ferrand

    collaborator OTHER
  • Hospices Civils de Lyon

    collaborator OTHER
  • Poitiers University Hospital

    collaborator OTHER
  • University Hospital, Angers

    collaborator OTHER_GOV
  • Centre Hospitalier Universitaire de Nīmes

    collaborator OTHER
  • Centre Hospitalier Universitaire de Nice

    collaborator OTHER
  • Nantes University Hospital

    collaborator OTHER
  • University Hospital, Montpellier

    collaborator OTHER
  • Centre Hospitalier Universitaire Dijon

    collaborator OTHER
  • University Hospital, Grenoble

    collaborator OTHER
  • Fondation Hôpital Saint-Joseph

    collaborator OTHER
  • CHU de Tours

    collaborator UNKNOWN
  • Centre Hospitalier Princesse Grace

    lead OTHER

Principal Investigators

  • Pierre HAUSFATER, MD-PhD · Assistance Publique - Hôpitaux de Paris

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-04-19
Primary Completion
2025-12-15
Completion
2026-03-30

Countries

  • France
  • Monaco

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05885529 on ClinicalTrials.gov