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Active clinical trials for "Intracranial Embolism and Thrombosis"

Results 1-7 of 7

NAUTILUS CE-mark Trial of the FLOWer Cerebral Embolic Protection Device

Aortic Valve StenosisIntracranial Embolism and Thrombosis

The purpose of this clinical study is to assess the safety, performance, and treatment effect of the use of the AorticLab FLOWer System, in preventing cerebral thromboembolic complications in patients with indication for a TAVI (Transcatheter Aortic Valve Implant).

Recruiting29 enrollment criteria

Magnetically Enhanced Diffusion for Acute Ischaemic Stroke (MEDIS) Trial

StrokeAcute8 more

The objective of the MEDIS study is to determine if subjects experiencing an Acute Ischaemic Stroke due to large vessel occlusion, treated with IV tPA combined with the MED procedure have a greater likelihood of recanalisation 30-90 minutes after the completion of tPA infusion than subjects treated with IV tPA (plus sham device). Safety of the MED System Procedure will be evaluated by the incidence of symptomatic PH-2 haemorrhagic transformation within 24 hours following the procedure. Lastly, a health economics study will be conducted to estimate health care costs for each treatment.

Suspended28 enrollment criteria

Thrombolysis and RIPC in Acute Ischemic Stroke

Acute Ischemic StrokeCerebral Embolism and Thrombosis

Remote ischemic postconditioning (RIPC) is suggested to protect the cerebral cell against ischemia in various settings. However, the effect of RIPC in patients with acute ischemic stroke who undergo thrombolysis has yet to be examined. In this single-center, randomized controlled trial, we examined the effect of RIPC on the resolution of nerve function deficient in response to thrombolysis. Patients in the RIPC group had five cycles of 5-min cuff inflation followed by 3-min deflation to the bilateral upper arm after thrombolysis. The primary endpoint was the recovery of nerve function deficient assessed by National Institutes of Health Stroke Scale(NIHSS), Activities of Daily Living(ADL), Modified Rankin Scale(mRS), CT cerebral perfusion imaging (CTP) and CT angiography(CTA). Secondary endpoints included the following: angiogenesis assessed by the level of vascular endothelial growth factor (VEGF), basic fibroblast growth factor (bFGF).

Completed10 enrollment criteria

Boston Area Anticoagulation Trial for Atrial Fibrillation (BAATAF)

ArrhythmiaAtrial Fibrillation6 more

To determine the benefits and risks of oral anticoagulant therapy in reducing embolic stroke and systemic emboli in patients with atrial fibrillation without rheumatic heart disease.

Completed1 enrollment criteria

Stroke Prevention in Sickle Cell Anemia (STOP 1)

AnemiaSickle Cell4 more

To reduce episodes of first time stroke by 75 percent in children with sickle cell anemia by the administration of prophylactic transfusion therapy.

Completed1 enrollment criteria

Transcranial Doppler (TCD) Ultrasound of Subjects Enrolled in BABY HUG - Ancillary to BABY HUG

Blood DiseaseAnemia3 more

To use transcranial Doppler (TCD) ultrasound to detect stroke risk in children with sickle cell disease.

Completed1 enrollment criteria

TCD Detection of Gas and Solid Micro-Emboli in Patients Undergoing Coronary Artery Bypass Grafting...

Intracranial Embolism and ThrombosisPostoperative Complications

The purpose of this study is to test the hypothesis that using three different techniques to anastomose coronary grafts to the aorta: partial occlusion, single cross clamp, or using the Heartstring anastomotic device, will change the amount of gas and solid microemboli as detected by the EmbodopR transcranial Doppler (TCD) system and consequently the neurocognitive performance of patients after coronary bypass operation.

Unknown status3 enrollment criteria
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