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The primary study outcome was anemia response.
The primary study outcome was the blood pressure measurements every minute for 11 minutes.
MDD symptoms were assessed weekly using a clinician-rated measure (Hamilton Depression Rating Scale; Ham-D); and neurocognition (working memory), at baseline and study outcome.
The primary study outcome was clinically diagnosed maternal peripartal infection: chorioamnionitis or endometritis.
However, assessment bias among investigators could have been avoided if the study outcome data had been collected by investigators who were blinded to group allocation.
The study outcome was development of a recurrence of ocular HSV disease documented by clinical examination.
Finally, we propose a number of future research directions based on the case study outcome.
The study outcome was compared with mapping and inventory results from other North American cities.
The studies were heterogeneous in design, swallowing assessment, and study outcome; therefore, we present findings descriptively.
The resulting correlation matrix shows the influence of the test setup on the study outcome.
The primary study outcome is time to incidence of a major CVD event.
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