Evaluation of Efficacy and Safety of Resuscitative Endovascular Balloon Occlusion of the Aorta with standardized protocol; A prospective observational study

Evaluation of Efficacy and Safety of Resuscitative Endovascular Balloon Occlusion of the Aorta with standardized protocol; A prospective observational study - Efficacy and Safety of Standardized REBOA protocol

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

JPRN

Registry ID

JPRN-UMIN000029760

Enrollment

150

Registered

2018-01-01

Start date

2018-01-01

Completion date

Unknown

Last updated

2026-06-29

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

Conditions

Refractory hemorrhagic shock

Interventions

None listed

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Refractory hemorrhagic shock undergoing REBOA

Exclusion criteria

Exclusion criteria: Age <15 years old The patients undergoing resuscitative thoraacotomy, elective cases, REBOA catheter placement without inflation

Design outcomes

Primary

Measure	Time frame
24 hour and 30 day mortality Transfusion within first 24 hours	—

Countries

Japan

Contacts

Public ContactYosuke Matsumura

Chiba University Graduate School of Medicine Department of Emergency and Critical Care Medicine

yousuke.jpn4035@gmail.com043-222-7171

Outcome results