Stroke Clinical Trials

Medtronic Evaluation of Multi-Electrode Phased RF Technology in Persistent Atrial Fibrillation

Alternatively, the study may stop early for futility if more than 6 procedure and/or device related strokes occur within the 30 day peri-procedural period prior to completing enrollment. Study subjects from all geographies will be followed for 6 months following their final ablation procedure, or official study closure defined as …

Vessel Wall Enhancement in Giant Cell Arteritis

They must be 50 years or older and have had cranial manifestations related to GCA including: visual symptoms, headache, temporal artery tenderness, jaw claudication, scalp tenderness, or stroke. Participants will be asked to complete an MRI scan within 2 weeks of enrollment and fill out questionnaires. Follow up visits will …

Mechanisms for Individual Differences in Hypertension in Obstructive Sleep Apnea

The purpose of this study is to compare the response to PAP treatment of patients with Obstructive Sleep Apnea (OSA) who have normal blood pressure to those with treated (that is taking medication or on a special diet) high blood pressure.

A Phase 2 Randomized Blinded study of Transcranial Magnetic Stimulation and Constraint Induced Language Therapy for the treatment of Chronic Aphasia

The Laboratory for Cognition and Neural Stimulation (LCNS) is currently recruiting individuals who have suffered from stroke and are now experiencing aphasia, a loss or impairment of language abilities, for a clinical trial. The purpose of this study is to determine if Transcranial Magnetic Stimulation (TMS), a form of non-invasive …

Efficacy of DE-MRI-Guided Fibrosis Ablation vs. Conventional Catheter Ablation of Atrial Fibrillation: The DECAAF II Study

You are being asked to participate in this study because you have atrial fibrillation and are planning to undergo an ablation procedure to treat this heart rhythm irregularity.

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