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Arteriovenous Malformations clinical trials

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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: NCT00590291 Terminated - Clinical trials for Coronary Artery Disease

Molecular Determinants of Coronaruy Artery Disease

GeneQuest
Start date: January 1995
Phase:
Study type: Observational

The purpose of this study is to discover genes that may cause Coronary Artery Disease (CAD) or Arteriovenous Malformation (AVM).

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: NCT00230685 Recruiting - Clinical trials for Telangiectasia, Hereditary Hemorrhagic

Case Notes Review on Patients With Hereditary Haemorrhagic Telangiectasia

Start date: January 2000
Phase:
Study type: Observational

This observational study is for individuals with Hereditary haemorrhagic telangiectasia and pulmonary arteriovenous malformations that are reviewed at the Hammersmith Hospital, London.

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.

NCT ID: NCT00001364 Completed - Clinical trials for Arteriovenous Fistula

Evaluation and Treatment of Patients Spinal Blood Vessel Abnormalities

Start date: June 2, 1993
Phase: N/A
Study type: Observational

Arteriovenous malformations (AVM) are abnormally formed blood vessels that can be located throughout the brain and spinal cord. Patients with abnormalities of the blood vessels located in and around the spinal cord can develop many neurological problems. Some problems include, weakness, pain, difficulty walking, paralysis, and even death. The treatment for these AVMs depends on their location, the type of malformation, the area of the spine involved, and the condition of the patient at the time of treatment. The treatment is aimed at stopping the neurologic problems from worsening and possibly correcting the existing problems. There are two commonly used treatments for AVMs, surgery and embolization (blocking off of blood flow to the AVM). However, researchers have limited experience treating these conditions because they are rare. In addition, it has been difficult to classify different kinds of AVMs and to develop new treatments for them. This study is designed to increase researchers understanding of AVMs by admitting and following patients diagnosed with the condition. By increasing the amount of patients studied diagnosed with spinal blood vessel abnormalities, researchers can begin to develop new management plans for patients with AVMs.