Study of trauma associated with the use of an automatic cardiac massager during cardiopulmonary resuscitation

Adverse events related to resuscitation with a mechanical chest compression device (MCCD): a prospective observational study - Adverse events due to mechanical chest compression device (MCCD)

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

JPRN

Registry ID

JPRN-UMIN000047074

Enrollment

800

Registered

2022-03-04

Start date

2022-04-01

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

Non-traumatic out-of-hospital cardiac arrest

Interventions

None listed

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Patients with non-traumatic out-of-hospital cardiac arrest who used LUCAS, a mechanical chest compression device

Exclusion criteria

Exclusion criteria: None

Design outcomes

Primary

Measure	Time frame
By combining clinical findings and CT image interpretation findings by a radiologist, a) skin damage, b) sternum / rib fracture, c) pneumothorax / hemothorax, d) presence or absence of parenchymal organ damage is evaluated.	—

Countries

Japan

Contacts

Public ContactTetsuya Sato

Tohoku University Hospital Emergency and Critical Care Medicine

t23jor@med.tohoku.ac.jp022-717-7489

Outcome results