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Mechanical External Compression for Human Cardiac Arrest -Nonrandomized non-Interventional Comparison Study-

Mechanical External Compression for Human Cardiac Arrest -Nonrandomized non-Interventional Comparison Study- - MECHANICS

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000006954
Enrollment
1590
Registered
2011-12-27
Start date
2012-01-01
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

out-of-hospital cardiopulmonary arrest

Interventions

None listed

Sponsors

Teikyo University School of Medicine, Department of Emergency Medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1) Patients who were experiencing cardiac arrest at the time of contact by ambulance team (2) Patients who underwent cardiopulmonary resuscitation by ambulance team (3) Patients not younger than 18 years and younger than 76 years (4) Patients in whom the first identified ECG waveform suggested pulseless electrical activity (PEA) *Regardless of existence or nonexistence of witness, regardless of with or without bystander cardiopulmonary resuscitation (CPR), and regardless of particulars of support by the ambulance team. (5) Patients judged to suffer endogenous OHCA at the medical organization to which the patient has been transferred (6) Patients for whom the ambulance team acted in an attempt to begin using an automatic chest compressor as soon as possible after confirming an initial ECG waveform (implementation within 3 minutes is desirable). * It does not matter whether use of the automatic chest compressor was started actually within 3 minutes.

Exclusion criteria

Exclusion criteria: (1) Patients who underwent electric shock by a layperson using an AED

Design outcomes

Primary

MeasureTime frame
The ratio of return of spontaneous circulation (ROSC) before hospital arrival shall be the primary outcome measure.

Secondary

MeasureTime frame
Survival at 1 month and survival at 1 month with minimal neurologic impairment, which was defined as Glasgow-Pittsburgh Cerebral Performance Category 1 (good cerebral performance) or 2 (moderate cerebral disability) shall be secondary outcome measures.

Countries

Japan

Contacts

Public ContactYasuo Takeuchi

Teikyo University Institute of Global Education

ytake@med.teikyo-u.ac.jp03-3964-1211

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026