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Blood Transfusion by Boston MedFlight Registry

Blood Transfusion by Boston MedFlight Registry

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04610814
Enrollment
500
Registered
2020-11-02
Start date
2019-11-01
Completion date
2024-12-31
Last updated
2021-09-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hemorrhagic Shock

Keywords

Blood transfusion, Pre-hospital care

Brief summary

The primary aim of this observational registry is to study the outcomes of patients with hemorrhagic shock transported by Boston MedFlight receiving blood products during transport.

Detailed description

Boston MedFlight, a critical care transport organization, based on a consortium of the academic medical centers in Boston, will begin carrying PRBC in 2019. The program is intended to provide BMF clinicians with 24-hour immediate access to appropriate blood products to be utilized if needed for patients following life-threatening illness or injury. The four fundamental goals of this program are: save lives' ensure transfusion safety; minimize blood product waste; and conduct continuous quality assurance. Our goal is to observationally evaluate this new protocol of administering blood products in the pre-hospital setting. We will collect data on patients with hemorrhagic shock being transported by Boston MedFlight, who receive or would have been eligible to receive pre-hospital blood transfusion by the inclusion criteria.

Interventions

None listed

Sponsors

Boston MedFlight
CollaboratorUNKNOWN
Boston Medical Center
CollaboratorOTHER
Tufts Medical Center
CollaboratorOTHER
Lahey Clinic
CollaboratorOTHER
Beth Israel Deaconess Medical Center
CollaboratorOTHER
Massachusetts General Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Adult patients who would be eligible to receive blood products; * systolic blood pressure \<90 mmHg * a shock index of \> 0.9 * clinical signs of shock as determined by the transport clinicians.

Exclusion criteria

* Age \< 18 years old

Design outcomes

Primary

MeasureTime frameDescription
30-day mortality30 days30-day all cause mortality

Countries

United States

Contacts

Primary ContactAngela Renne
ARENNE@MGH.HARVARD.EDU617-643-2440

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026