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Careful endotracheal suctioning was performed before the protocol was started.
One of the biggest recent wins for OpenID Connect was actually announced earlier this week (before the protocol was fully ratified).
Month 12 results for subjects who were enrolled before the protocol was amended were also summarized.
Two refusals (one patient and one family member) were in the early stages of recruitment before the protocol was amended; therefore these two patients were offered and accepted the fast-track service.
The study protocol was approved by the Institutional Review Board at each of the 3 investigative sites, and written informed consent was obtained from each study participant before the protocol was initiated.
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Staff and patients evaluated pain management before and after the protocol was instituted.
Before activation, the protocol was approved by the National Cancer Institute, Division of Cancer Prevention and the GOG Human Research Committee, and annually by the Institutional Review Board at each of the participating institutions.
Before silencing experiments, the protocol was adjusted to ensure a minimum of 80% of RNA knockdown assessed by qPCR.
4 Written informed consent was obtained from individual patients before participation and the protocol was approved by each Institutional Review Board.
Written informed consent was obtained from each subject before inclusion and the protocol was approved by the French Ethics Committee for Human Research and by the National Committee for Data Processing and Freedom.
Before beginning the study the protocol was discussed with the hospital ethical committee.
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