Optimizing advanced MRI techniques for brain and mental health conditions
OPTIMIZATION of AVANCED MR SEQUENCES for BRAIN STUDIES in VOLUNTEERS (HEALTHY and PATIENTS)
This study is testing new MRI techniques to see if they can provide clearer images and better measurements for people with brain and mental health conditions.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 300 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Centre Hospitalier St Anne Academic / other |
| Locations | 1 site (Paris) |
| Trial ID | NCT05618990 on ClinicalTrials.gov |
What this trial studies
This observational study focuses on enhancing advanced MRI sequences to improve image quality, reduce artifacts, and optimize acquisition times on a new 3T MRI unit. The primary goal is to validate these optimized MR protocols using healthy volunteers and patients, ensuring reliable quantitative measurements. Secondary objectives include assessing the feasibility of these protocols and conducting reproducibility studies to confirm their effectiveness in clinical and cognitive neuroscience research.
Who should consider this trial
Good fit: Ideal candidates for this study are adults aged 18 and older who are covered by social security and can provide written consent.
Not a fit: Patients with any contraindications for MRI, such as claustrophobia or pregnancy, will not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved MRI imaging techniques that enhance diagnosis and treatment monitoring for brain tumors and mental disorders.
How similar studies have performed: While this study focuses on optimizing MRI techniques, similar studies have shown promise in improving imaging protocols, suggesting potential for success.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * 18 ans * Covered by social security * For women in age of procreation, under efficient contraception * Written consent Exclusion Criteria: * Any MR contraindication * Claustrophobia * Pregnancy * Under judiciary protection
Where this trial is running
Paris
- OPPENHEIM Catherine — Paris, France (Recruiting)
Study contacts
- Study coordinator: Khaoussou SYLLA
- Email: k.sylla@ghu-paris.fr
- Phone: 01 45 65 76 78
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.