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Influence of MMP on Brain AVM Hemorrhage

Influence of Matrix Metalloproteinase on Brain Arteriovenous Malformation Hemorrhage

Status
Completed
Phases
Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00783523
Enrollment
33
Registered
2008-10-31
Start date
2008-03-31
Completion date
2010-12-31
Last updated
2013-08-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Arteriovenous Malformations, Brain Aneurysms, Cavernous Angiomas

Brief summary

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.

Detailed description

* 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.

Interventions

DRUGDoxycycline or Placebo

Randomized to Doxycycline 100mg 2x/day or Placebo 2x/day for 1 or2-weeks pre-operatively.

Sponsors

University of California, San Francisco
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
PREVENTION
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
13 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* 13 years or older * Female patients of child bearing age using barrier-type birth control * Creatinine no greater than 2.0 mg/di * Alanine aminotransferase (ALT) no greater than 2 times upper limit of normal * WBC count at least 3,800/mm3 * BMI within 50% of normal

Exclusion criteria

* Allergy to tetracycline * Unstable medical illness (unstable angina, advanced cancer, etc) over the last 30 days * Female patients of child-bearing age not using effective birth control (barrier) * History of vestibular disease (except benign positional vertigo) * History of noncompliance with treatment or other experimental protocols * Patients taking other antibiotics * History of systemic lupus erythematosis * Patients who are immunocompromised Patients with clinically significant hepatic dysfunction

Design outcomes

Primary

MeasureTime frame
Our primary aim is to perform a pilot study to document the effect of doxycycline therapy to decrease MMP expression in the vascular malformation tissue.1 to 2-week pre-operative

Secondary

MeasureTime frame
Our secondary aims are: (1) To explore whether plasma MMP-9 levels can be used as a marker for MMP-9 inhibition in the vascular malformation lesional tissue1 to 2-week pre operative

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026