Skip to content

A Prospective Study of Early Mechanical Stabilization and Bleeding in Disruption of the Pelvic Ring

A Prospective Study of Early Mechanical Stabilization and Bleeding in Disruption of the Pelvic Ring

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03977168
Acronym
EMS-BIND
Enrollment
600
Registered
2019-06-06
Start date
2019-05-17
Completion date
2022-09-30
Last updated
2022-08-30

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

Conditions

Pelvic Fracture

Brief summary

The objective of this study is to evaluate the effect of earlier placement of Circumferential Pelvic Compression (CPC) on resuscitative measures required for life-threatening pelvic ring injuries and to guide the development of future efficacy trials of three advanced resuscitation techniques (surgical pelvic packing, angioembolization, REBOA).

Interventions

PROCEDUREApplication of circumferential pelvic compression (CPC) device

Application of circumferential pelvic compression (CPC) device used at any time within 24 hours of injury

Sponsors

Major Extremity Trauma Research Consortium
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 64 Years
Healthy volunteers
No

Inclusion criteria

* Patient age between 18 and 64 years, inclusive; * Severe blunt or blast traumatic injury; * Young-Burgess APC-2 and 3, LC-3, vertical shear, and combined mechanism of injury (CMI) (Tile B and C patterns; OTA codes 61-B and 61-C); * Circumferential pelvic compression (CPC) device used at any time within 24 hours of injury. * Patient must speak either English or Spanish

Exclusion criteria

* Arrival to hospital of definitive care more than 6 hours after injury; * Ballistic pelvic injury, other than from a blast mechanism; * Time of CPC placement not recorded; * Time of injury and time of EMS dispatch unknown; * Use of medical anti-shock trousers (MAST); * Confirmed dead on arrival to hospital

Design outcomes

Primary

MeasureTime frameDescription
Pelvic stabilization and resuscitative techniques24 hoursWe will document any techniques used to stabilize and/or resuscitate the pelvic injury within the first 24 hours
Blood products24 hoursWe will document the volume of any blood products given within the first 24 hours following injury

Secondary

MeasureTime frameDescription
Ventilator days24 hoursNumber of days that patient spends on a ventilator will be documented
ICU days24 hoursNumber of days spent in the ICU will be documented
GCS (Glascow Coma Score)24 hoursThe GCS is a neurological scale to assess for brain injury. The score is composed of three parts: eyes, verbal and motor. Each component has a different scale. Eyes (1-4), verbal (1-5) and motor (1-6). The sum of all three components result in the overall GCS score (3-15). The higher the score, the less likelihood of brain injury
Length of hospital stay24 hoursNumber of days spent in the hospital will be documented
Blood loss24 hoursTotal blood volume loss will be calculated within the first 24 hours following injury

Other

MeasureTime frameDescription
Mortality1 monthAny deaths that occur between index hospitalization and 30 days post-injury will be documented

Countries

United States

Outcome results

None listed

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