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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05929144
Other study ID # 23-0030
Secondary ID 2023-A00398-37
Status Recruiting
Phase N/A
First received
Last updated
Start date May 5, 2023
Est. completion date July 2028

Study information

Verified date May 2023
Source University Hospital, Caen
Contact Géraldine Poisnel, PhD
Phone 0231470206
Email poisnel@cyceron.fr
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The Inserm NeuroPresage team has been using MRI for more than 20 years in the study of normal ageing and memory pathologies to further the understanding and the characterization of early diagnosis and the cerebral substrates of cognitive deficits in patients, particularly in the context of neurodegenerative diseases. Two years ago, a new 3T MRI camera was installed at the Cyceron centre. It is more efficient and should make it possible to obtain better quality images and/or to reduce the time required to acquire these images. In this context, it seems important to test the different sequences that we classically use in our studies, or that we plan to implement in our next studies (learning and text retrieval fMRI task), in order to optimize them, with a view to integrating them in our future studies.


Recruitment information / eligibility

Status Recruiting
Enrollment 40
Est. completion date July 2028
Est. primary completion date July 2028
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Healthy volunteers of legal age - Affiliation with a social security scheme or beneficiary of such a scheme - Signing of the protocol informed consent - For women of childbearing age or capacity, a urine pregnancy test before inclusion Exclusion Criteria: - Protected persons in accordance with articles L. 1121-5 to L.1121-8 of the Public Health Code: protected adults, pregnant and nursing women - Presence of contraindications to MRI examination without contrast agents injection - Presence of a chronic neurological or psychiatric condition (including substance use disorder) - History of brain disease (vascular, degenerative, malformative, tumour, or head trauma with loss of consciousness for more than one hour) - Current or recent use of medications that may interfere with imaging (psychotropic drugs, antihistamines with anticholinergic action, antiparkinsonian drugs, benzodiazepines including muscle relaxants, long-term steroidal anti-inflammatory drugs, antiepileptic drugs, central painkillers)

Study Design


Related Conditions & MeSH terms


Intervention

Other:
MRI sequences testing
Testing different MRI sequences in order to optimize them

Locations

Country Name City State
France GIP Cyceron Caen

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Caen

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Optimization of MRI sequences TR, TE, Flip Angle, asset phase, asset slice parameters During MRI sessions
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