EDGAR

Emergency Data Gathering and AlphaStroke Refinement

Project Summary:

Assess signal strength and the diagnostic clinical performance of an experimental device

Population:

Patients 18 years and older with acute neurologic deficits (NIHSS > 2) presenting to ED within 24 hours of symptom onset.

Outcomes:

Capture signals of adequate quality in an ED environment.

Enrollment:

Stage 1 ended Feb. 2019 | Stage 2 began March 2019

Study Team:

Misty Ottman, BSN, CCRP | Henry Wang, MD, MPH, MS | Ryan Huebinger, MD| Richard Gordon, MD | Emergency Medicine Research Assistants

Presentations:

AHA HealthTech | Podcast


Funding and Collaborators:

Memorial Hermann - Texas Medical Center Logo

Forest Devices Logo


Site Project Leadership:

Paulina Sergot, MD
Paulina Sergot, MD

Dr. Sergot has a longstanding interest in furthering the diagnosis and care of neurological emergencies, such as stroke and traumatic brain injury. Her research focus was spurred by her experience as a Howard Hughes Research Fellow, where she investigated neurogenesis after acute stroke. She has been a Co-Investigator of Transforming Research and Clinical Knowledge in TBI (TRACK-TBI). She is a Co-I of the Neurological Emergencies Treatment Trials Network (NETT) and is a site Co-I of the Strategies to Innovate Emergency Care Clinical Trials (SIREN) network. She is also involved in device development to aid in the acute diagnosis of concussion and stroke.