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Primary assessment was performed for major loss of reduction and iatrogenic ulnar nerve injury.
The primary assessment was the quantitative evaluation of gait markers.
The primary assessment was A1C after 16 weeks of treatment.
The primary assessment was American College of Rheumatology (ACR) 20 response at week 16.
The patients were treated for 6 weeks and the primary assessment was performed at 12 weeks.
The primary assessment was change in HbA1c after 26 weeks of treatment.
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Primary assessment is generally provided through the use of fixed cameras and most surveillance systems use pan-tilt-zoom (PTZ) cameras.
Most primary assessments are made in conditions with limited facilities and therefore there may be reasonable considerations against its use in some situations.
The primary efficacy assessment was the mean change from baseline assessed at week 8 in total IDS-C30 score for adjunctive armodafinil 150 mg/day versus adjunctive placebo as analyzed by mixed-model repeated measures (MMRM).
The primary efficacy assessment was the sum of pain intensity differences at 30 min (SPID30) postdose.
The primary efficacy assessment was the change in ADHD-RS-IV total score from baseline to endpoint.
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