Skip to main content
Clinical Trials/JPRN-jRCT1032230589
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.

Registry
who.int
Start Date
January 23, 2024
End Date
TBD
Last Updated
2 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
mekawa Motoyuki

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

Similar Trials