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Arteriovenous Malformations clinical trials

View clinical trials related to Arteriovenous Malformations.

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NCT ID: NCT02436213 Completed - Clinical trials for Hereditary Hemorrhagic Telangiectasia

Cardiopulmonary Exercise Testing to Evaluate Pulmonary AVMs

Start date: April 2011
Phase: N/A
Study type: Interventional

Pulmonary arteriovenous malformations (PAVMs) are a rare vascular condition affecting the lungs. PAVMs lead to low blood oxygen levels, yet are very well tolerated by patients. This study will examine the exercise capacity of PAVM patients using formal cardiopulmonary exercise tests performed on a stationary bicycle.

NCT ID: NCT02378883 Completed - Clinical trials for Arteriovenous Malformations

Apollo™ Onyx™ Delivery Microcatheter Post Market Safety Study

Start date: May 18, 2015
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the safety of the Apollo™ Onyx™ Delivery Microcatheter used for delivery of the Onyx™ Liquid Embolic System during brain arteriovenous malformation (AVM) embolization procedures.

NCT ID: NCT02314377 Completed - Clinical trials for Brain Arteriovenous Malformation

Bevacizumab Therapy for Brain Arteriovenous Malformation

Start date: June 2016
Phase: Phase 1
Study type: Interventional

Bevacizumab Therapy for brain arteriovenous malformation that is not amenable to surgical intervention.

NCT ID: NCT02180958 Completed - Clinical trials for Cerebral Arteriovenous Malformations

Evaluation of ONYX in ENDOVASCULAR Treatment of Cerebral AVMs

cAVM
Start date: July 2014
Phase:
Study type: Observational [Patient Registry]

To assess safety and efficacy of ONYX treatment for cAVM:

NCT ID: NCT02085278 Completed - Clinical trials for Brain Arteriovenous Malformation

Safety of Apollo Micro Catheter in Pediatric Patients

Start date: February 2014
Phase: N/A
Study type: Interventional

This is a clinical trial/study for patients diagnosed with brain arteriovenous malformation (AVM). An AVM is an abnormal connection between the arteries and veins of the brain. Patients considered for this trial are 21 years and younger with AVM suitable for embolization treatment (a procedure used to block the abnormal connection between the arteries and veins of the brain) with Onyx Liquid Embolic System (Onyx LES) or TruFill n-Butyl Cyanoacrylate (n-BCA) Liquid Embolic System (both are liquid substances used in the embolization procedure to block the abnormal connection).

NCT ID: NCT01856842 Completed - Clinical trials for Pulmonary Arteriovenous Malformations

Reperfusion of Pulmonary Arteriovenous Malformations After Embolotherapy

Start date: April 2013
Phase: N/A
Study type: Interventional

AVMs are abnormal collections of blood vessels which can occur in any part of the body including the lungs. These blood vessels are weakened and can rupture anytime causing bleeding which can be massive, leading to life-threatening conditions. Pulmonary AVMs occur in about 40% of patients with HHT. Each patient may have an average of 5 AVMs .Rupture of the AVM can lead to massive bleeding in the lung, stroke and infection of the brain. In order to prevent these complications, patients with HHT are routinely examined for pulmonary AVMs and treatment with embolization is recommended. AVMs have a main blood vessel or artery supplying blood to the collection of blood vessels. The way to treat AVMs is cut off their blood supply through a process called embolization. Embolization is a standard medical procedure which is done to stop or prevent hemorrhage (bleeding) from an AVM. It involves blocking the artery that supplies blood to the AVM by inserting a foreign body, into the blood vessel supplying blood to the AVM. Standard devices used for embolization include coils (made of stainless steel or platinum). These devices usually have a good success rate for blocking the artery that supplies blood to the AVM. However, a few AVMs that are embolized by standard devices may reopen over time. This is called reperfusion and will require repeat embolization procedures. For embolization of pulmonary AVMs at St. Michael's Hospital, the Nester coil is used. In this study, we would like to compare the Nester coil with a new coil device called the Interlock Fibered IDC Occlusion System. Both coils are approved for use in Canada, however the cost of the IDC coil limits its use at this hospital. Compared to the Nester coil, the IDC coils are made so that they can be removed or repositioned if they are not placed correctly. The coil also allows tighter packing which helps prevent reperfusion. This study will compare the success rate of embolization between the Interlock™ Fibered IDC™ Occlusion System (IDC coil) and the Nester coil.

NCT ID: NCT01689402 Completed - Brain Neoplasms Clinical Trials

MRI for the Early Evaluation of Acute Intracerebral Hemorrhage

Start date: April 2012
Phase:
Study type: Observational

What happens in the borderzone of a cerebral hemorrhage remains widely onknown and furhter the best timing for doing MR to look for vascular pathology in cerebral hemorrhage has not yet been determined. In this study we do acute MRS, a non-invasive imaging mathod to detemine the biochemsty in the border zone and structural MRI for vascular malformation. We repeat structural MRI after 8 weeks.

NCT ID: NCT01677624 Completed - Clinical trials for Hypervascular Tumor and Arteriovenous Malformation

A Multicenter, Open-label Study for E7040 in Japanese Subjects With Hypervascular Tumor and Subjects With Arteriovenous Malformation

Start date: August 2012
Phase: Phase 3
Study type: Interventional

To evaluate the efficacy and safety of transcatheter arterial embolization with E7040 in Japanese subjects with hypervascular tumor or arteriovenous malformation

NCT ID: NCT01381952 Completed - Aneurysm Clinical Trials

Image Quality and Radiation Dose in Angiography

Start date: June 2011
Phase: N/A
Study type: Interventional

ClarityIQ is a novel X-ray imaging technology, that combines advanced real-time image noise reduction algorithms, with state-of-the-art hardware to reduce patient entrance dose significantly. This is realized by anatomy-specific optimization of the full acquisition chain (grid switch, beam filtering, pulse width, spot size, detector and image processing engine) for every clinical task individually. Furthermore, smaller focal spot sizes and shorter pulses are used, which are known to positively influence image quality . The final effect on the clinical image quality is investigated in this study.

NCT ID: NCT01347307 Completed - Meningioma Clinical Trials

Stereotactic Body Radiotherapy for Spine Tumors

Start date: September 2008
Phase: N/A
Study type: Interventional

This study will evaluate the local control rate as well as acute and late toxicity rates of stereotactic body radiotherapy (SBRT) for the treatment of spine metastases and benign spine tumors.