Stroke Clinical Trials in New York, New York
19 studies are recruiting for stroke in New York, New York right now. Each one is listed on ClinicalTrials.gov, the public registry the research teams themselves file with. TrialBoost is not a doctor, a research site, or a study sponsor: the research team decides who takes part.
Search these by distance from you
Studies now recruiting
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Treatment of Acute Ischemic Stroke (ReMEDy2 Trial)
This is a Phase 2/3 study evaluating the safety and efficacy of DM199 (rinvecalinase alfa) in treating participants with moderate stroke severity, who present within 24 hours of Acute Ischemic Stroke (AIS) onset due to small and medium vessel occlusions. This study focuses on participants with limi…
- Stage
- Phase 2
- Ages
- 18 to 90
- Site
- Northwell Health Physician Partners - Neurology at Lenox Hill, New York, New York
- Locations
- 86 in total
- Run by
- DiaMedica Therapeutics Inc
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Telerehabilitation In The Home After Stroke
The purpose of this research study is to evaluate whether telerehabilitation targeting arm movement, when added to usual care, improves arm function and reduces global disability after stroke, compared to usual care alone. Patients with arm weakness due to stroke that happened in the past 90-150 da…
- Stage
- Not phased
- Ages
- 18 to 80
- Site
- Icahn School of Medicine at Mount Sinai, New York, New York
- Locations
- 27 in total
- Run by
- University of California, Los Angeles
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Treatment With Endovascular Intervention for STroke Patients With Existing Disability
TESTED will compare the risks and benefits of endovascular thrombectomy (EVT) to medical management (no EVT) in ischemic stroke patients who have a blockage in one of the large blood vessels in the brain and have a moderate-to-severe disability prior to their stroke.
- Stage
- Not phased
- Ages
- 18 and older
- Site
- Icahn School of Medicine at Mount Sinai, New York, New York
- Locations
- 35 in total
- Run by
- University of Cincinnati
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Validation of Early Prognostic Data for Recovery Outcome After Stroke for Future, Higher Yield Trials
VERIFY will validate biomarkers of upper extremity (UE) motor outcome in the acute ischemic stroke window for immediate use in clinical trials, and explore these biomarkers in acute intracerebral hemorrhage. VERIFY will create the first multicenter, large-scale, prospective dataset of clinical, tra…
- Stage
- Not phased
- Ages
- 18 and older
- Site
- The Mount Sinai Hospital, New York, New York
- Locations
- 45 in total
- Run by
- Yale University
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A Digital Intervention for Post-Stroke Depression and Executive Dysfunction
Individuals with stroke commonly experience both depression and cognitive difficulties. The goal of this study is to evaluate the efficacy of a treatment that combines a digital therapeutic (an iPad-based cognitive training program) with learning cognitive strategies. The hypotheses are that this t…
- Stage
- Phase 2
- Ages
- 50 to 79
- Site
- Weill Cornell Medical Center, New York, New York
- Run by
- Weill Medical College of Cornell University
-
Carotid Implants for PreveNtion of STrokE ReCurrEnce From Large Vessel Occlusion in Atrial Fibrillation Patients Treated With Oral Anticoagulation
Patients with atrial fibrillation (AF) who have had a prior stroke are at very high risk of recurrent ischemic stroke. About 40% of these strokes are due to large emboli which result in large cerebral vessel occlusion (LVO). This randomized control trial aims to address this unmet need by testing w…
- Stage
- Not phased
- Ages
- 18 and older
- Site
- Weill Cornell Medical Center, New York, New York
- Locations
- 21 in total
- Run by
- Javelin Medical
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Cognition and Imaging With Tigertriever
The objective of the COGNITIVE Study is to evaluate whether successful reperfusion with Tigertriever is associated with cognitive benefit.
- Stage
- Not phased
- Ages
- 18 to 75
- Site
- Westchester Medical Center, New York, New York
- Locations
- 3 in total
- Run by
- Rapid Medical
-
Music Listening for Mental Health Recovery After Stroke
This study aims to explore whether listening to music intentionally can support the mental health of people recovering from a stroke. The question the investigators aim to answer is: Can intentional music listening improve emotional well-being in stroke survivors? And if so, what kinds of changes m…
- Stage
- Not phased
- Ages
- 50 to 90
- Site
- New York University, New York, New York
- Run by
- New York University
-
Clevidipine for the Antihypertensive Treatment of Acute Intracerebral Hemorrhage
The aim is to compare the rate of hypertensive subjects with ICH who reach SBP target with stability within 60 minutes of enrollment, among patients treated with IV clevidipine with those treated with alternate IV antihypertensive regimen.
- Stage
- Not phased
- Ages
- 18 to 100
- Site
- Icahn School of Medicine at Mount Sinai, New York, New York
- Locations
- 20 in total
- Run by
- Zeenat Qureshi Stroke Institute
-
Mobile Cognitive Behavioral Therapy for Stroke
This study aims to assess the feasibility and acceptability of "MAYA", a mobile cognitive behavioral therapy app for anxiety and mood disorders, in adults who have had a stroke.
- Stage
- Not phased
- Ages
- 40 to 79
- Site
- Weill Cornell Medicine, New York, New York
- Run by
- Weill Medical College of Cornell University
-
GORE® CARDIOFORM Septal Occluder and Antiplatelet Medical Management for Reduction of Recurrent Stroke in Patients With Patent Foramen Ovale (PFO): the REDUCE Post Approval Study
This study will assess the safety and effectiveness of GORE® CARDIOFORM Septal Occluder in a post approval setting and evaluate the quality of operator education and training and transferability of trial experience to a post-market setting.
- Stage
- Not phased
- Ages
- 18 to 70
- Site
- Columbia University Medical Center/NYPH, New York, New York
- Locations
- 45 in total
- Run by
- W.L.Gore & Associates
-
Diagnostic Performance Study of the EMVision Emu™ Brain Scanner in the Detection of Intracranial Hemorrhage in Suspected Stroke Patients
The purpose of this research is to evaluate a new investigational device for the diagnosis of stroke, the EMVision emu™ Brain Scanner. Stroke is the result of a blood clot stopping the normal flow of blood in the brain (ischaemic stroke) or a breakage in a blood vessel causing bleeding in the brain…
- Stage
- Not phased
- Ages
- 22 and older
- Site
- Mount Sinai West, New York, New York
- Locations
- 8 in total
- Run by
- EMVision Medical Devices Ltd
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Pilot/Pivotal Study of DBS+Rehab After Stroke
The RESTORE Stroke Study will evaluate the safety and effectiveness of DBS+Rehab for treating arm weakness and reduced function after a stroke.
- Stage
- Not phased
- Ages
- 21 and older
- Site
- NYU Langone Health, New York, New York
- Locations
- 10 in total
- Run by
- Enspire DBS Therapy, Inc.
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Comparison of Anti-coagulation and Anti-Platelet Therapies for Intracranial Vascular Atherostenosis- Magnetic Resonance Imaging
CAPTIVA-MRI is an observational multimodal MR imaging study that is ancillary to the CAPTIVA trial [a 3-arm, double-blind Phase III trial conducted at approximately 115 StrokeNet sites randomizing patients with stroke attributed to 70-99% intracranial atherosclerotic stenosis (ICAS) to aspirin plus…
- Stage
- Not phased
- Ages
- 18 and older
- Site
- NYP Columbia University Medical Center, New York, New York
- Locations
- 28 in total
- Run by
- Yale University
-
Genetic and Environmental Risk Factors for Hemorrhagic Stroke
The purpose of this study is to find risk factors for hemorrhagic stroke.
- Stage
- Not phased
- Ages
- 18 and older
- Site
- Columbia University, New York, New York
- Locations
- 7 in total
- Run by
- State University of New York at Buffalo
-
Anticoagulation for New-Onset Post-Operative Atrial Fibrillation After CABG
The primary objective of this study is to evaluate the effectiveness (prevention of thromboembolic events) and safety (major bleeding) of adding oral anticoagulation (OAC) to background antiplatelet therapy in patients who develop new-onset post-operative atrial fibrillation (POAF) after isolated c…
- Stage
- Phase 3
- Ages
- 18 and older
- Site
- Columbia University Medical Center, New York, New York
- Locations
- 106 in total
- Run by
- Icahn School of Medicine at Mount Sinai
-
MyHand 2: An Active Hand Orthosis for Stroke Patients
This study is designed to further develop and test the hardware and software components of the MyHand device based on user feedback and results from our pilot study. The goal is to refine the device so that is more effective and easier for stroke patients to use to increase their hand function.
- Stage
- Not phased
- Ages
- 18 and older
- Site
- Columbia University Irving Medical Center, New York, New York
- Run by
- Columbia University
-
SDOH-Homecare Intervention Focus Team (SHIFT) Trial to Improve Stroke Outcomes
Primary Goal: To test the hypothesis that among stroke patients 18-75 years with ≥3 SDOH risk factors, SHIFT will improve: (1) functional outcomes as measured by the SIS (Primary Outcome), (2) physiological outcomes as measured by changes in blood pressure and cognition, (secondary outcomes) and (3…
- Stage
- Not phased
- Ages
- 18 to 75
- Site
- Columbia University Medical Center, New York, New York
- Run by
- Columbia University
-
Transcranial Direct Current Stimulation (tDCS) With Verb Network Strengthening Treatment (VNeST) in Chronic Aphasia
The purpose of this study is to assess changes in language abilities of participants with chronic, post-stroke aphasia following an 8-week therapy period combined with brain stimulation. The investigators use a stimulation method called transcranial direct current stimulation (tDCS). The investigat…
- Stage
- Not phased
- Ages
- 21 to 80
- Site
- City University of New York, New York, New York
- Run by
- City University of New York
How to read this page. Every study here comes from ClinicalTrials.gov, the public registry that research teams are required to file with. We have summarised each one in plain language and shown where it is running. We have not changed what any study says it is doing.
What TrialBoost is. We help people find research that might suit them, and, if they ask us to, we pass their details to the research team running it. We are not a doctor, a research site, or a study sponsor, and we do not decide who takes part in anything. Joining costs nothing and you can change your mind at any point.
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