The aim of this prospective study is to reveal the natural history of symptomatic hemorrhage in adult patients with cerebral cavernous malformation with the goal of informing the treatment plan.
Cerebral cavernous malformation Patients with newly diagnosed, cerebral cavernous malformation who will visit one of the study centers during the period from June 2016 to December 2017. Patients would be eligible for enrollment if they were 18 years of age or older and had at least 1 cerebral cavernous malformation. If the patient had multiple cavernous malformations, index cavernous malformation would be enrolled. Index lesion will be determined according to the criteria. * Index lesion decision criteria I. Symptomatic II. Asymptomatic (priorities are as follows) 1. Previous bleed 2. Brain stem location 3. Deep nuclei (thalamus, caudate, basal ggl, hypothalamus) 4. Periventricular 5. Largest All patients who would visit a study center during the enrollment period and meet these criteria will be asked to join the study. The cohort will consists of patients who agree to participate. Target population of this study is 228 patients.
Study Type
OBSERVATIONAL
Enrollment
228
KangWon National University Hospital
Chuncheon, Gangwon-do, South Korea
Gyeongsang National University Hospital
Jinju, Gyeongsangnam-do, South Korea
HUMC-Chuncheon Sacred Heart Hospital
Chuncheon, Kanwon, South Korea
DongGuk University
Ilsan, Kyungkido, South Korea
Symptomatic hemorrhage
hemorrhage due to rupture of cavernous malformation
Time frame: 5 year
Symptomatic hemorrhage
hemorrhage due to rupture of cavernous malformation
Time frame: 1 year
All hemorrhagic event including radiologic rupture + newly appeared neurologic symptom
hemorrhage without symptom
Time frame: 1 year
All hemorrhagic event including radiologic rupture
all hemorrhagic events
Time frame: 5 year
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