Analyzing brain images in stroke patients
Analysis of Brain Diffusion Tensor Image in Stroke Patients
Bundang CHA Hospital · NCT06047223
This study looks at brain scans of stroke patients to see how their individual traits affect brain function and compares their blood test results and neurological abilities at the time of the scan.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 80 (estimated) |
| Ages | 20 Years and up |
| Sex | All |
| Sponsor | Bundang CHA Hospital (other) |
| Locations | 1 site (Seongnam-si, Gyeonggi-do) |
| Trial ID | NCT06047223 on ClinicalTrials.gov |
What this trial studies
This observational study aims to analyze brain diffusion tensor images in stroke patients to confirm the characteristics of functional anisotropy values based on individual patient traits. It will compare hematologic indicators and neurological function levels at the time of imaging. The study utilizes magnetic resonance imaging (MRI) to gather data on stroke patients and their conditions.
Who should consider this trial
Good fit: Ideal candidates are adults aged 20 years or older with a history of stroke.
Not a fit: Patients with severe medical conditions or those with devices affected by MRI will not benefit from this study.
Why it matters
Potential benefit: If successful, this study could enhance understanding of stroke characteristics and improve patient management.
How similar studies have performed: While this approach is observational, similar studies using MRI in stroke patients have shown promising results.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: 1. Adults aged 20 years or older with a history of stroke 2. After hearing a detailed explanation of this study and fully understanding it, the subject or legal representative voluntarily decides to participate and agrees in writing to observe the precautions Exclusion Criteria: Patients who meet one or more of the following cannot participate in the study. 1. Those with severe medical conditions such as unstable conditions in the cardiovascular system, digestive system, respiratory system, endocrine system, etc., and those with poor general health 2. In the case of a person with impaired consent, a person without a guardian 3. Patients who have devices that may be affected by MRI, such as pacemakers, spinal cord stimulators, cochlear implants, VP shunts, and nerve stimulators, inserted into the body 4. Other cases where the researcher judges that participation in this study is not suitable (This study is not an interventional study, and patients who are participating in other clinical trials or studies or who have participated in other clinical trials or studies within the past 30 days can also participate in this study.)
Where this trial is running
Seongnam-si, Gyeonggi-do
- CHA Bundang Medical Center, CHA University — Seongnam-si, Gyeonggi-do, Korea, Republic of (RECRUITING)
Study contacts
- Principal investigator: Minyoung Kim, M.D., Ph.D. — Bundang CHA Hospital
- Study coordinator: Hyun Jung Oh, BS
- Email: a210525@chamc.co.kr
- Phone: +82 031 780 6003
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.
Conditions: Stroke