APPRAISE 2.0: Live Trial of the APPRAISE Trauma Decision Support System
Launched by ANDREW TOMAS REISNER · Nov 2, 2023
Trial Information
Current as of June 26, 2025
Recruiting
Keywords
ClinConnect Summary
The APPRAISE 2.0 trial is studying a new software system designed to help doctors make quick decisions when treating patients with serious injuries in the emergency department. This pilot study aims to see how well the software works during real-time use, whether it distracts or confuses doctors while they are treating patients, and to gather initial data that will help plan a larger study in the future.
To be eligible to participate, patients must be 18 years or older and be in the "Acute" area of the emergency department, which is where patients with critical health concerns are treated. They should have a clear concern for an acute injury. However, patients who are prisoners, pregnant, or have any concerns about using the software will not be included in the study. Participants in this trial can expect to have their treatment guided by both the software and the medical team, helping to improve care for trauma patients.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • Adult (≥18 yrs) Emergency Department (ED) patient
- • Triaged to the "Acute" area of the ED. (The "Acute" area is the designated area for ED patients with potential or established critical illness. Triage to Acute is a routine ED operation that is performed based on departmental guidelines and the professional judgement of an experienced triage nurse).
- • Clinical concern for acute injury (based on either an explicitly chief complaint of acute injury, or clinical team with documented concern for acute injury as a relevant part of patient presentation).
- Exclusion Criteria:
- • Prisoners
- • Patients known to be pregnant, based on patient report, physical exam, or bedside ultrasound
- • Patients wearing an "EFIC Opt-Out" bracelet
- • Any concern about the suitability of the software system for a specific patient by any clinician involved in the patient's ED care, or by the patient themselves (or by any LAR \[lawfully authorized representative\] of the patient).
About Andrew Tomas Reisner
Andrew Tomas Reisner is a dedicated clinical trial sponsor with a strong commitment to advancing medical research and improving patient outcomes. With a focus on innovative therapies and evidence-based practices, Reisner leads initiatives that prioritize rigorous scientific methodology and ethical standards. His extensive experience in clinical development and collaboration with multidisciplinary teams ensures the effective design and execution of trials. By fostering partnerships within the healthcare community, Reisner aims to translate research findings into practical applications that enhance healthcare delivery and patient care.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Boston, Massachusetts, United States
Patients applied
Trial Officials
Andrew Reisner, MD
Principal Investigator
Mass. General Hospital
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported