Skip to main content
OpenTrials
Completed

NCT Number: NCT03062306

Chest Compression and Cerebral Oxygenation During Cardiopulmonary Resuscitation

In recent years, monitorizations during Cardiopulmonary Resuscitation (CPR) are inadequate to show the sufficiency of cerebral oxygenation. During CPR, insufficient chest compressions have critical importance for neurological results and life quality after the return of spontaneous circulation (ROSC).

Completed

Looking for future studies?

Notify Me

Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Mehmet Akif YAZAR

Nevşehir, 50100, Turkey (Türkiye)

About this study

The Near-Infrared Spectroscopy (NIRS), which is used in measuring the cerebral tissue oxygenation is one of the latest technologies that allow the measurement of brain oxygen saturation. With this study, the issue of whether sufficient cerebral oxygenation is provided during CPR applied to patients that have Cardiac Arrest (CA) will be investigated, and the effect of CPR on the patient prognosis after ROSC will be examined. In this study, the aim is to investigate whether sufficient oxygenation is provided in synchronization with chest compressions during CPR; and to test the regional brain tissue saturation with rSO2 measurement, and the prognosis with Full Outline of UnResponsiveness (FOUR) Score in patients with ROSC.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • All patients undergoing cardiac arrest in intensive care unit

Exclusion criteria

  • Head injury and intracranial bleeding
  • Cerebral ischemic vascular event
  • Pulmonary diseases that may affect blood-oxygen levels
  • Below the age of 18

Treatment and study plan

Primary outcomes

  1. The levels of regional brain tissue oxygen saturation (rSO2) providing with chest compressions during Cardiopulmonary Resuscitation (CPR)

    Time frame: About six month

    The data will be obtained by using the Near Infrared Spectroscopy (NIRS) Device and will be recorded rSO2 measurement during the resuscitation of the Cardiac Arrest (CA) patients

Secondary outcomes

  1. Change from baseline in consciousness on Full Outline of UnResponsiveness (FOUR) Score at one week

    Time frame: For a week after ROSC

    The patient's consciousness will be evaluated by FOUR score in patients with ROSC

Sponsors and collaborators

Lead sponsor

Nevsehir Public Hospital

Other Gov

Registry information

Official study title

Can Sufficient Cerebral Oxygenation be Provided in a Synchronized Manner With Chest Compression During Cardiopulmonary Resuscitation?

Acronym: CPR

Important dates

Study start
2017
Primary completion
2017
Study completion
2018
First posted
Feb 23, 2017
Registry last updated
Feb 22, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.