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All enrolled study patients provided their written informed consent for enrolment into the study.
31 patients enrolled, study period 7 days.
Written informed consent was obtained from all enrolled study participants.
SS, CJC, DSB, and KTT enrolled study subjects.
The intent-to-treat population is defined as all enrolled study participants.
NSC, CAM enrolled study women and provided cytological and histological diagnoses.
The demographic and disease characteristics of the enrolled study participants are presented in Table 1.
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We use a three stage approach to enroll study participants.
A few years ago, my father enrolled to study law.
100 patients enrolled, mean study period 4 days.
Participants were enrolled by study investigators.
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