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Patients (141) requesting emergency contraception and lacking contraindications were offered entry in the study.
Full informed consent was obtained before entry into the study.
Of these animals 23 provided data that was considered suitable for entry into the study.
Before his entry into the study, Phil was importing the drug from a generic manufacturer from his native South Africa.
Time since entry into the study was used as the underlying time metric.
At entry to the study, all participants received a clinical examination and a blood draw.
within 2 months before the entry to the study.
Patients were trastuzumab-naive at entry to the study.
All participants gave informed consent upon entry to the study.
All patients signed informed consent before entry into the study.
Two hundred eighteen patients were screened for entry into the study.
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