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Clinical Trials/NCT07527949
NCT07527949Not yet recruitingNot Applicable

PASTRAMI : Patient-specific Statistics for Microstructure-augmented Connectomics

Rennes University Hospital2 sites in 1 country100 target enrollmentStarted: September 1, 2026Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Not yet recruiting
Sponsor
Enrollment
100
Locations
2
Primary Endpoint
Measures of brain microstructure

Study Overview

Brief Summary

Traumatic brain injury (TBI) represent a major public health issue, accounting for approximately 1.5 million hospital admissions annually across the European Union and 160,000 cases in France. They are a significant cause of mortality and disability, with serious consequences for patients and their families. Predicting functional outcomes remains complex due to the heterogeneity of brain injuries, whether primary or secondary, as well as the mechanisms involved, particularly neuroinflammation. This difficulty is particularly pronounced for moderate to severe TBI, for which current predictive tools are still limited.

The PASTRAMI project proposes to utilise diffusion magnetic resonance imaging (MRI) to identify biomarkers associated with axonal lesions in the white matter. This technique enables the analysis of brain microstructure and the reconstruction of neural connections (connectome), thereby offering innovative prospects for improving the prediction of functional recovery.

This is a prospective, multicentre, interventional study involving 100 patients aged between 18 and 60 years with moderate to severe traumatic brain injury. The primary objective is to assess the prognostic value of brain microstructural measures at baseline, by correlating them with the GOSE functional score at 1 year. Secondary objectives include the analysis of mortality, functional outcome, quality of life, and early physiological factors influencing progression.

Patients will undergo a standard MRI scan supplemented with additional sequences for prognostic purposes, without any change to their therapeutic management. The associated risks are minimal and relate primarily to the MRI scan. No immediate individual benefit is expected, but the results could improve our understanding of brain lesions and optimise future management.

The total duration of the study is 48 months. The expected outcomes include better characterisation of lesions and improved predictive tools, contributing to more appropriate clinical decisions.

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Other
Masking
None

Eligibility Criteria

Ages
18 Years to 60 Years (Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Aged 18 to 60
  • Admitted for moderate to severe non-penetrating head injury (with a Glasgow Coma Scale score ≤ 12)
  • On mechanical ventilation and under continuous sedation
  • Enrolled in a social security program
  • Whose family has been informed and has signed a voluntary, informed, written consent form

Exclusion Criteria

  • History of head trauma, stroke, or neurodegenerative diseases
  • A decision to limit active treatment has already been made
  • Quadriplegia
  • Contraindications to MRI
  • Protected individuals (adults under legal protection [judicial protection, guardianship, conservatorship], individuals deprived of liberty, pregnant women [self-reported], breastfeeding women, and minors).

Arms & Interventions

Additional imaging studies for prognostic purposes

Experimental

Intervention: Measures of brain microstructure (Other)

Outcomes

Primary Outcomes

Measures of brain microstructure

Time Frame: baseline

Correlation between the GOSE score at 1 year and measures of brain microstructure at baseline

GOSE score

Time Frame: 1 year

Correlation between the GOSE score at 1 year and measures of brain microstructure at baseline

GOSE score (Glasgow Outcome Scale Extended) [between 1 and 8 (higher score mean a better outcome)]

Time Frame: 1 year

Correlation between the GOSE score at 1 year and measures of brain microstructure at baseline

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
Rennes University Hospital
Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (2)

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