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Clearly it is inappropriate to treat fellow eyes with different treatments if the outcome of the study is assessed at the patient level unless perhaps treatment for each eye is over different time periods.
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All rating scales used in the study are assessed and validated in Danish.
Rutting behaviour of SMA mixtures prepared in the study was assessed by wheel-tracking test.
Evolution of hemodynamic and respiratory levels during the study was assessed using a linear mixed model adjusted for time.
On the other hand, the study was assessed not to have deficits that are described below for studies with a low level of evidence.
Compatibility of BS with various excipients used during the study was assessed using DSC and FTIR techniques.
Compliance and drug exposure during the study were assessed by tablet counting.
The percentage change in hemoglobin between baseline and the end of the double-blind phase of the study was assessed.
The power of the study was assessed 0.99.
The study was assessed as a service evaluation by UCL Joint Research & Ethics Committee Office.
The pathological data described in the study were assessed on the initial core biopsy.
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