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After informed consent was obtained, enrolled patients had clinical exam findings documented on a standardized form and underwent point-of-care lung ultrasound examination.
After written informed consent was obtained, enrolled patients were randomly assigned to have their wounds irrigated with SS or TW, using a sequentially numbered plastic-wrapped sterile bowl.
The primary randomized intervention study from which these data were obtained enrolled a total sample of 719 ACS patients who had been hospitalized in five mid-Michigan hospitals [ 23].
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Methods: After Ethical Committee approval was obtained, we enrolled patients with age > 18 years, scheduled for thoracic surgery and OLV with double-lumen tube in lateral decubitus.
This study protocol was approved by the ethics committee of our hospital, and informed consent was obtained from enrolled patients.
JAK participated in the design of the study, obtained funding, enrolled patients, and participated in drafting the manuscript.
In line with the Helsinki Declaration [ 22], only mothers from whom informed consent was obtained were enrolled for the study.
All human blood samples were obtained from enrolled individuals with the approval of institutional review board at the University of Florida.
All human blood samples were obtained from enrolled individuals with the approval of the institutional review board (IRB) at the University of Florida.
After obtaining consent, enrolled patients were switched to a Servo-i ventilator (Maquet, Solna, Stockholm, Sweden).
Consistent with Tri-Council policy, a waiver of consent was obtained to enroll all NH residents experiencing emergency transfers [ 21].
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