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KT participated in the design if the study and coordination and helped to draft the manuscript and as a surgeon she operated the pigs.
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If two OR were presented in the study and if they concerned different exposures/populations, both were included.
RNs asked patients who visited them fore lifestyle discussions if they wanted to participate in the study and if the interviewer could call them.
Informed, written consent was obtained from each patient participating in the study and if required from their parents.
IF conceived the study and helped to draft the manuscript.
AMF, BOP, IF conceived the study and revised the manuscript.
This is however only true if the studies and especially information on the reference tests used are sufficiently detailed.
This is however only true if the studies and especially information on the reference tests used are described in sufficient detail.
If eligible for the study (and to undergo CEA), they were given an explanation of the purpose of the study and were required to give written consent.
The patient receives information about the study and if willing to participate, the patient registers online.
Callers were provided with a brief description of the study, and if interested, underwent phone screening.
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