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Arteriovenous Malformations clinical trials

View clinical trials related to Arteriovenous Malformations.

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NCT ID: NCT00972790 Completed - Epilepsy Clinical Trials

Scalp Nerve Blocks for Post-Craniotomy Pain

Start date: March 2010
Phase: N/A
Study type: Interventional

The objective of this study is to demonstrate that scalp nerve blocks ("scalp freezing"), performed at the end of supratentorial brain surgery, will reduce post-operative pain, opioids side effects, and the time required for post-anaesthesia care unit (PACU)/Intensive Care Unit (ICU) and hospital discharge.

NCT ID: NCT00857662 Completed - Clinical trials for Brain Arteriovenous Malformations

Study Comparing Onyx and TRUFILL in Brain Arteriovenous Malformations (AVMs)

Start date: May 2001
Phase: Phase 2
Study type: Interventional

Test whether AVMs treated with Onyx is equivalent to treatment with n-BCA. Success is defined as an AVM size reduction greater than 50%

NCT ID: NCT00783523 Completed - Clinical trials for Arteriovenous Malformations

Influence of MMP on Brain AVM Hemorrhage

Start date: March 2008
Phase: Phase 1
Study type: Interventional

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.

NCT ID: NCT00603694 Completed - Clinical trials for Trigeminal Neuralgia

Hippocampal Radiation Exposure and Memory

Start date: September 2007
Phase: N/A
Study type: Observational

Neurocognitive impairment as a result of gamma knife radiosurgery has not been well studied and is poorly understood. Radiosurgery to the base of skull for the treatment of benign and malignant disorders may consequently impair memory function. There is a need to evaluate changes in memory function that may be associated with such exposures. In this pilot study, we will investigate changes in hippocampal-dependent memory function in 10 patients receiving a low SRS dose to the hippocampus. We will also investigate such changes in a no-dose control group and a high-dose control group. This study will provide preliminary estimates of variance in memory changes associated with radiation exposure, and will then permit us to design future studies with the appropriate sample size justification.

NCT ID: NCT00577213 Completed - Clinical trials for Arteriovenous Malformations

Diagnosis of Hemangiomas and Vascular Malformations

Start date: February 2007
Phase: N/A
Study type: Observational

To develop a non-invasive, simple and affordable, measurement technique to differentiate hemangiomas from subtypes of VMS. The purpose of this study is to determine the best office based diagnositc instrument for differentiating the subtype of vascular lesions. The instrument must be simple and affordable so it can be used by primary car physicians in the doctor office. The procedure will be based on non-invasive and unharmful measurements that will be compared to the diagnosis from specialized physicians in this field and the final pathology.

NCT ID: NCT00573872 Completed - Neoplasm Clinical Trials

A Phase II Study of Spinal Radiosurgery

RAD0408
Start date: April 2005
Phase: N/A
Study type: Interventional

Phase I of the study (motion and quality assurance [QA] study) is being used to determine intrafraction target motion and define quality assurance procedures for single fraction spinal radiosurgery. The Phase II portion of the study is being used to estimate the palliative response (pain or relief of neurologic symptoms) and local control for single fraction radiosurgery delivered with TomoTherapy and to assess the acute and late toxicity of spinal radiosurgery.

NCT ID: NCT00389935 Completed - Clinical trials for Hereditary Hemorrhagic Telangiectasia

Thalidomide Reduces Arteriovenous Malformation Related Gastrointestinal Bleeding

TAG
Start date: October 2006
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine whether Thalidomide is effective in the treatment of arteriovenous malformations in the gastrointestinal tract.

NCT ID: NCT00389181 Completed - Clinical trials for Arteriovenous Malformations, Cerebral

A Randomized Trial of Unruptured Brain AVMs

ARUBA
Start date: October 2006
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine if medical management is better than invasive therapy for improving the long-term outcome of patients with unruptured brain arteriovenous malformations.

NCT ID: NCT00243893 Completed - Clinical trials for Arteriovenous Malformations

Tetracycline-Derivatives for Treatment of Cerebral Arteriovenous Malformations and Aneurysms

Start date: July 2004
Phase: Phase 1
Study type: Interventional

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.

NCT ID: NCT00004648 Completed - Clinical trials for Telangiectasia, Hereditary Hemorrhagic

Studies of Hereditary Hemorrhagic Telangiectasia

Start date: May 1996
Phase: N/A
Study type: Observational

OBJECTIVES: I. Examine screening modalities for pulmonary vascular arteriovenous malformation (PAVM) in individuals with endoglin mutations. II. Examine the prevalence of cerebral arteriovenous malformations (CAVM) in individuals with hereditary hemorrhagic telangiectasia (HHT). III. Investigate whether modifier genes exist that determine which individuals with HHT due to an endoglin mutation develop PAVMs and which develop CAVMs. IV. Investigate the frequency of cardiac valve abnormalities in individuals affected with HHT due to an endoglin mutations.