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Study on the application of 7.0T ultra-high field magnetic resonance in the surgical diagnosis and treatment of glioma

Study on the application of 7.0T ultra-high field magnetic resonance in the surgical diagnosis and treatment of glioma

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2000036816
Enrollment
Unknown
Registered
2020-08-25
Start date
2020-10-01
Completion date
Unknown
Last updated
2020-09-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

glioma

Interventions

glioma parients:take 7t MR preoperation

Sponsors

Huashan Hospital Affiliated to Fudan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: (1) men and women aged 18-70 years; (2) Preoperatively based on existing 3T magnetic resonance sequences (including but not limited to T1, T2, T2 Flair, T1 enhancement, DWI, etc.); (3) Persons with full prior informed consent prior to surgery and without surgical taboos; (4) The patient completes a full set of cognitive assessment before surgery; (4) Patients without severe liver, kidney, cardiopulmonary and mental disorders; (5) No symptoms of high cranial pressure such as headache and vomiting, no dehydration treatment; (6) MMSE more than 26 points, KPS more than 80 points, able to cooperate with out-of-hospital inspectors.

Exclusion criteria

Exclusion criteria: 1. The subjects refused to participate in the study; 2. Metal objects, including pacemakers, defibrillators, heart stents, and artificial hearts, were installed in the subjects; Dirty valves, postoperative metal clips, drug perfusion devices implanted into the body, any electronic devices implanted into the body, nerve stimulators, bone growth stimulators, any other type of biostimus, intravascular embolism rings, filters, lower cavity vein filters, electroencular recorders, metal seams Joints, bullets in the body, shrapnel or iron sand particles, fixed steel plates, steel nails, ? silks, artificial prosthetics or joints, penis prosthesis, hearing aids, cochlear implants, middle ear grafts, metal foreign objects in the eyes, prosthetic eyes, Active dentures, braces and head and face implants; 3. Those who have incomplete clinical data or claustrophobia, etc., are not able to follow the experimental steps or are unable to cooperate; 4. Subjects combined with severe medical conditions, such as 2 times the normal upper limit of ALT, 6 times the normal upper limit of Cr, severe pulmonary inseptibility or arrhythmic disorders, etc.; 5. Subjects combined with other serious intracranial diseases requiring emergency treatment; 6. Subjects combined mental illnesses, such as schizophrenia, severe depression, etc.; 7. The subjects combined the pregnancies; 8. People with frequent seizures who are unable to cooperate; 9. Other clinical trials common during the same period.

Design outcomes

Primary

MeasureTime frame
MRI examination;

Countries

China

Contacts

Public ContactLiang Chen

Huashan Hospital Affiliated to Fudan University

chenlianghs@126.com+86 13311735889

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026