A Study Of The STAT Relay™ Tray For Safe Transfers During Emergency Trauma Care
Overview
Tab Title Description
Study type
ObservationalDescribes the nature of a clinical study. Types include:
- Observational study — observes people and measures outcomes without affecting results.
- Interventional study (clinical trial) — studies new tests, treatments, drugs, surgical procedures or devices.
- Medical records research — uses historical information collected from medical records of large groups of people to study how diseases progress and which treatments and surgeries work best.
Study IDs
Site IRB
- Rochester, Minnesota: 26-010695
About this study
The purpose of this study is to evaluate the feasibility and safety of integrating the STAT Relay™ Tray into routine care of adult Red-Level and Yellow-Level and Yellow-Level Trauma patients.
Participation eligibility
Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Contact the study team to discuss study eligibility and potential participation.
Inclusion Criteria:
Patient participants: age 18 years or older; Red-Level and Yellow-Level Trauma activation; care in a participating pilot location; STAT Relay™ Tray used during care based on treating-team clinical judgment; and consent/authorization requirements satisfied according to the IRB-approved plan.
Staff participants: age 18 years or older; Mayo Clinic staff member who directly interacted with the STAT Relay™ Tray during patient care; willing to complete the voluntary study evaluation.
Exclusion Criteria:
Patient is younger than 18 years.
Clinical judgment, patient condition, or operational criteria indicate that tray use is inappropriate.
Patient requires transfer to a setting where the pilot workflow cannot be supported before meaningful study observation can occur.
Prisoner status is identified.
Required patient or legally authorized representative consent/authorization for inclusion of research data is not obtained, when required by the IRB-approved plan.
Staff member did not directly interact with the tray, or does not wish to participate in the anonymous survey.
Note: Other protocol defined Inclusion/Exclusion Criteria may apply.
Eligibility last updated 09/04/2026. Questions regarding updates should be directed to the study team contact.
Participating Mayo Clinic locations
Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.
| Mayo Clinic Location |
Status |
|
Rochester, Minn.
Mayo Clinic principal investigator Daniel Stephens, M.D. |
Open for enrollment |
|
More information
Publications
Publications are currently not available