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Fifty patients with cardiac arrest induced by ACS and 31 patients with acute myocardial infarction (AMI) who did not require cardioversion or cardiopulmonary resuscitation were enrolled in the study, as were 40 healthy volunteers.
The initial patient was enrolled in April 2012, and a total of 71 patients had been enrolled in the study as of the end of March 2014, when the enrollment period was closed.
The patients enrolled in the study, as is traditional in early experiments with a treatment, were the sickest of cancer patients, those not expected to live for more than a few weeks to a few months in any case.
Healthy adults with no known ocular diseases were enrolled in the study as controls.
Eligible participants were then enrolled in the study as described above.
Healthy volunteers (n = 18) were enrolled in the study as controls.
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At age 14 years 10 137 children enrolled in the study at birth and 444 enrolled as part of phases 2 and 3 were eligible for follow-up, and were sent questionnaires.
Its purpose is to monitor the level of activity in the subjects enrolled in the study, both as an outcome measure as well as an activity-monitoring strategy for all subjects.
The control sites invited persons, who met the study eligibility criteria, to enroll in the study as the control group.
A randomization process with a 2 3 ratio was selected to convince patients to enroll in the study, as they would have a higher chance of being included in a treatment group rather than a control group.
In accordance with CHREB guidelines, written consent will be obtained from each individual prior to being enrolled in the study formally as a participant, and prior to any testing.
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