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Image quality evaluation of low-dose new orbit CBCT

Not Applicable
Conditions
Patients undergoing postoperative CBCT examinat ion in neuro-endovascular treatment
Registration Number
JPRN-jRCTs032220133
Lead Sponsor
Matsumaru Yuji
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
40
Inclusion Criteria

1) Cases in which postoperative examination by C BCT was performed after neuro-endovascular treat ment and then consent was given to additional ex amination (about 2 minutes) by CBCT using a new trajectory.
2) Cases aged 20 years or older at the time of consent acquisition

Exclusion Criteria

1) cases difficult to fix the head during imaging
2) cases of acute stroke
3) pregnant women
4) othrer cases that the investigator or doctors deems inappropriate

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Artifact
Secondary Outcome Measures
NameTimeMethod
detection of cerebral hemorrhage or subarachnoid hemorrhage<br>brain parenchymal contrast<br>white matter and gray matter identification
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