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For logistic reasons it was not possible to assess blindly for control or preterm status.
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The size of the resultant tumors was assessed blindly every day, and the tumor area (mm2) was assessed by measuring the maximum diameter with a caliper.
Surveys were numbered and assessed blindly; the scorers did not know whose survey they were scoring or whether they were evaluating a pre- or post-survey.
The effects of HDLs were assessed blindly 24 h later by evaluating the neurological deficit and mortality and by measuring both infarct volume and hemorrhagic transformation.
For ischemic lesion size determination, on each slice, the infarcted area was assessed blindly and delineated by the relative paleness of histological staining tracing the area on a video screen.
Slides were coded and assessed blindly by a pathologist (SGH).
The focus scores were assessed blindly by two different examiners and the mean scores were determined.
Drug exposures were assessed blindly regarding the case or control status, through contacts with patients, their family and/or their physicians.
The neurological deficit after MCAO or NMDA application was assessed blindly by two investigators using a four-point scoring system established for rats [34], [35] and mice [33], [36].
Specimens were assessed blindly and independently by two pathologists.
All graft kidney slides were assessed blindly by a pathologist.
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