Effect of interpossed abdominal compression cardiopulmonary resuscitation on end tidal co2 and 24 Hour Survival of Cardiopulmonary Arrest Patient

Comparison of the Effect of IAC-CPR and Current CPR Methods on ETCO2 and 24 Hour Survival of Cardiopulmonary Arrest Patient

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT2014010216033N1

Enrollment

Registered

2014-01-22

Start date

2013-12-22

Completion date

Unknown

Last updated

2018-02-22

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

Conditions

cardiac arrest. Cardiac Arrest

Interventions

Intervention 1: in intervention group after confirmation of cardiac arrest and endotracheal intubation Interpossed Abdominal Compression Cardiopulmonary Resuscitation is performing. Interventi

Treatment - Other

in intervention group after confirmation of cardiac arrest and endotracheal intubation Interpossed Abdominal Compression Cardiopulmonary Resuscitation is performing.

in control group after confirmation of cardiac arrest and endotracheal intubation current Cardiopulmonary Resuscitation is performing.

Eligibility

Sex/Gender

All

Age

18 Years to 85 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: confirmation of cardiopulmonary arrest; nonTraumatic cardiopulmonary arrest; Age between eighteen to eighty-five years; Existence of endotracheal tube; No history of abdominal aortic aneurysm; No recent abdominal surgery; No pregnancy; exclusion criteria: Suspected pregnancy; Inability to intubation; Return of spontaneous circulation before beggining of resuscitation

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
End Tidal CO2. Timepoint: During the intervention. Method of measurement: Capnograph.;Return of spontaneos Circulation. Timepoint: After the intervention. Method of measurement: check of pulse and blood pressure.;24 hours survival. Timepoint: 24 hour after intervention. Method of measurement: By questionnaire.	—

Secondary

Measure	Time frame
Side effect. Timepoint: During and 24 hours after intervention. Method of measurement: By observation and examination.	—

Countries

Iran (Islamic Republic of)

Contacts

Public Contactjavad malekzadeh

Mashhad University of Medical Sciences

malekzadehj@mums.ac.ir00

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026