Assessing cognitive function in patients with focal brain injuries

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study focuses on understanding cognitive deficits associated with focal brain injuries by building a comprehensive database of behavioral responses during cognitive tasks. It targets patients with specific types of brain lesions, such as those resulting from strokes or surgical resections, to analyze how these lesions affect various cognitive functions. The study aims to collect extensive data to clarify the relationship between lesion characteristics and cognitive performance, ultimately enhancing our understanding of brain function and recovery.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Male and female patients, 18-70 years old
* A single, focal anatomical lesion of a given cerebral territory (post vascular, post surgical resection) documented by MRI
* Intellectual ability and understanding of instructions compatible with the cognitive tasks to be performed

Exclusion Criteria:

* Patient deprived of liberty
* Somatic disorder likely to affect cognitive abilities
* Pregnant or nursing woman

Where it's running

• University Hospital, Grenoble
  Grenoble, France Recruiting

Study contacts

• Principal investigator: Philippe Kahane, MD, PhD — University Hospital, Grenoble
• Study coordinator: Philippe Kahane, MD, PhD
• Email: pkahane@chu-grenoble.fr
• Phone: +33 476 765 488

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.