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Completed

NCT Number: NCT00243893

Tetracycline-Derivatives for Treatment of Cerebral Arteriovenous Malformations and Aneurysms

The purpose of this pilot study is to investigate the use of minocycline and doxycycline as medical therapy for inoperable or partially treated arteriovenous malformations (AVMs) and giant aneurysms.

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Key information

Age range

13 year–80 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Primary location

University of California

San Francisco, California, 94143, United States

About this study

Arteriovenous malformations (AVMs) are a treatable cause of stroke in young adults. The processes by which AVMs and giant aneurysms grow in size and spontaneously bleed are unknown. The primary reason to treat AVMs and aneurysms is to guard against intracranial bleeding.

This pilot study will examine the use of two common antibiotics-minocycline and doxycycline-as medical therapy for inoperable or partially treated AVMs and giant aneurysms. These drugs, which are tetracycline derivatives, can reduce the levels of a family of enzymes, called matrix metalloproteases, that degrade tissue and thereby cause a reduction in the risk of spontaneous bleeding from AVMs or aneurysm-which is the main cause of stroke associated with these disorders. The enzymes can contribute to weaknesses in the wall of blood vessels and may increase the risk of the vessel wall rupturing and causing spontaneous bleeding.

This trial also will show that taking minocycline and doxycycline over an extended period in this patient population is safe and well tolerated. Results from this study could help plan future studies to benefit patients with abnormal blood vessels prone to bleeding in their brains.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Giant aneurysms or brain arteriovenous malformations (BAVM)
  • Female patients of child bearing age using effective birth control, males
  • Creatinine no greater than 2.0 mg/dl
  • ALT no greater than 2 times upper limit of control

Exclusion criteria

  • Unstable medical illness
  • Contraindications to Tetracycline
  • History of vestibular disease, (except benign positional vertigo)
  • Prior tetracycline use within 2 mos of baseline visit.
  • History of noncompliance with treatment or other protocols
  • History of systemic lupus
  • Patients not eligible for MRI

Treatment and study plan

Minocycline

Drug

Take minocycline 50mg BID x2 years. Labs drawn at baseline, then every-6 months. MRI is done at baseline and completion of study.

Doxycycline

Drug

Take doxycycline 50mg BID x2 years. Labs drawn at baseline, then every-6 months. MRI is done at baseline and completion of study.

Primary outcomes

  1. MRI will be done baseline and post treatment.

    Time frame: 2 years

  2. MMP levels are being followed q 6-mos.

    Time frame: Patients called weekly for 1st-3 months, then every 6-months until completion of study

  3. Drug levels are being followed q 6-mos.

    Time frame: Patients called weekly for 1st-3 months, then every 6-months until completion of study

Sponsors and collaborators

Lead sponsor

University of California, San Francisco

Other

Collaborators

  • National Institute of Neurological Disorders and Stroke (NINDS)

Registry information

Important dates

Study start
2004
Primary completion
2008
Study completion
2008
First posted
Oct 25, 2005
Registry last updated
Oct 9, 2013

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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