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Clinical Studies

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  • Geriatric Emergency Department Collaborative (GEDC) Data Repository Rochester, Minn.

    The main purpose of the database is to create and maintain an analysis-ready limited data set from multiple healthcare centers, including continuously updated data from electronic medical records and a linked prospective dataset which was previously collected through an NYULH IRB-approved multi-site research study (i24-00287 - GEARSS).

Closed for Enrollment

  • An Observational, Multicentre Study To Evaluate The Feasibility Of A Novel Mobile Health Monitoring Platform To Capture Patient-centered Outcomes Measures Among Patients With Heart Failure (HF) Jacksonville, Fla., Rochester, Minn. The Food and Drug Administration (FDA) recognizes the importance of developing patient-centric endpoints that are relevant to patients beyond mortality and hospitalizations. Patients with HF have reduced function capacity and quality of life (QoL) and hence it is imperative to explore interventions that impact endpoints that directly measure how a patient feels or functions on a daily basis. Recently, new mobile health technologies have emerged as clinical tools and offer an opportunity to overcome these challenges in measuring functional capacity and recording symptoms. These technologies are able to capture and integrate data from disparate sources from individual patients reflecting their functional status and symptomatology. These data can potentially serve as surrogate endpoints for approval of new HF therapies. In this study, the investigators will test the feasibility of a novel mobile health monitoring platform to capture patients' physiology, functional capacity and assessment of quality of life.
  • Real-World Data to Assess Variation in Opioid Prescribing and Use for Acute Pain in Diverse Populations Rochester, Minn.

    This is a prospective observational cohort study.

    This study will address important gaps in knowledge that hamper the development of evidence-based guidelines for acute pain management by prospectively following patients for 180 days and collecting detailed information on patients’ self-reported experience of pain and their corresponding analgesic use.

    This study will invite opioid-naïve patients receiving an opioid prescription for the treatment of acute pain in primary or urgent care, an emergency department, or a dental office. Opioid naive patients are those who self-report no opioid use in the prior 6 months. For the purpose of the study, acute pain is defined as pain that started less than 8 weeks before entry in the study. The study will follow consented patients prospectively for 180 days, tracking their pain and treatment patterns using a novel patient-centered health data sharing platform – Hugo – that will consolidate data from patient-reported outcomes, pharmacy records, and electronic health records.
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