JPRN-jRCT1032230589
Not yet recruiting
Phase 4
Efficacy of stereotactic radiosurgery based on three-dimensional rotational angiography for cerebrovascular malformation: A prospective interventional trial
mekawa Motoyuki0 sites60 target enrollmentJanuary 23, 2024
Overview
- Phase
- Phase 4
- Intervention
- Not specified
- Conditions
- Brain arteriovenous malformation
- Sponsor
- mekawa Motoyuki
- Enrollment
- 60
- Status
- Not yet recruiting
- Last Updated
- 2 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Inclusion criteria are as follows:
- •(1\) Individuals in whom a brain arteriovenous malformation (BAVM) has been identified by head MRI examination.
- •(2\) Age: Individuals who are 5 years old or older but under 80 years old at the time of consent acquisition.
- •(3\) Gender: Not specified.
- •(4\) Individuals who have received sufficient explanation about participating in this study, have understood it fully, and have given their written consent freely either personally or through a representative.
- •(5\) Individuals who are able to attend outpatient visits in accordance with the research implementation schedule.
Exclusion Criteria
- •Individuals meeting any of the following exclusion criteria will be excluded from the study:
- •(1\) Those with large lesions (volume over 20cm^3\) requiring multiple treatments (staged treatment).
- •(2\) Individuals unable to give consent or assent due to impaired consciousness.
- •(3\) Those with serious renal dysfunction.
- •(4\) Individuals with a history of serious drug allergies such as anaphylactic shock or a history of serious side effects.
- •(5\) Those who have participated in clinical trials or research studies and taken experimental drugs within 4 weeks prior to consent acquisition.
- •(6\) Individuals planning to undergo radiation therapy for the same lesion or other intracranial lesions during the period from the time of consent acquisition until the end of the study period.
- •(7\) Pregnant individuals or those suspected to be pregnant.
- •(8\) Others whom the research director or participating physician deems inappropriate for participation in this study
Outcomes
Primary Outcomes
Not specified
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