Reoxygenation After Cardiac Arrest (REOX Study)

Completed

Conditions studied: Cardiac Arrest

In brief

The broad objective of this study is to test the association between hyperoxia exposure after resuscitation from cardiac arrest and outcome. Our overarching hypothesis is that hyperoxia after ROSC is associated with increased oxidative stress and worsened neurological and cognitive outcomes.

Key facts

Study ID

NCT01881243

Run by

The Cooper Health System

People needed

280

Starts

2013-06-01

Expected to finish

2017-06-01

Last updated by the study team

2019-11-25

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Age >17 years
• Cardiac arrest
• Return of spontaneous circulation
• Not following commands immediately after ROSC
• Endotracheal intubation
• Clinician intent to treat with therapeutic hypothermia (or absence of clinician intent to withhold therapeutic hypothermia)

You may not qualify if…

• Presumed etiology of arrest is trauma
• Presumed etiology of arrest is hemorrhage
• Presumed etiology of arrest is sepsis
• Permanent resident of nursing home or other long-term care facility
• Any other condition, that in the opinion of the investigator, would preclude the subject from being a suitable candidate, e.g. end stage chronic illness with no reasonable expectation of survival to hospital discharge

Where it is running

• Indiana University/ Methodist Hospital — Indianapolis, Indiana, United States
• Beth Israel Deaconess Medical Center — Boston, Massachusetts, United States
• University of Mississippi Medical Center — Jackson, Mississippi, United States
• Cooper University Hospital — Camden, New Jersey, United States
• Hospital of the University of Pennsylvania and Penn Presbyterian Medical Center — Philadelphia, Pennsylvania, United States

Full record on ClinicalTrials.gov

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