Arteriovenous Malformations Clinical Trial
Official title:
Influence of Matrix Metalloproteinase on Brain Arteriovenous Malformation Hemorrhage
Brain vascular malformations, including arteriovenous malformations (AVM), cavernous
malformations (CVM) and aneurysms, are a source of life-threatening risk of intracranial
hemorrhage. The etiology and pathogenesis are unknown. There is no medical therapy presently
available. Prevention of spontaneous intracerebral hemorrhage (ICH) is the primary reason to
treat brain vascular malformations. The goal of this study is to: begin pilot studies to lay
the groundwork for future clinical trials to develop medical therapy to decrease ICH risk.
Matrix metalloproteinases (MMPs) regulate the extracellular matrix in association with
various hemorrhagic brain disorders. MMP-9 has been most consistently associated with
vascular wall instability and hemorrhagic brain disorders. Doxycycline, a non-specific MMP
inhibitor, may enhance vascular stability, thus reducing the risk of spontaneous hemorrhage
in brain vascular malformations by decreasing MMP-9 activity.
- Doses will be randomized by the Pharmacy Department at UCSF for Doxycycline 100 mg/BID
and Placebo BID. These will be prepared in blister-packs.
- Depending on enrollment/surgery date, patients will take medication either one to two
weeks before surgery. Patients will be assigned to a treatment group according to a
random table.
- Each patient will be initially provided with a 1 or 2-week supply of drug in blister
packs. The patient will take the final dose of study drug on the morning of surgery.
Baseline labs will be obtained and then again at time of surgery along with a piece of
surgical tissue.
;
Allocation: Randomized, Intervention Model: Single Group Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Prevention
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