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In the trial by Kono et al [ 11], patients were enrolled using a predetermined randomization list along with sealed envelopes.
Using a predetermined randomization table, subjects were assigned to one of two groups for 20 min daily treatment for 1 month – direct visual observation of another person's lower limbs and feet moving coupled with the subject moving his phantom limbs and feet mimicking the same movements (n = 11) or mental visualization of moving the subject's phantom limbs and feet (n = 9).
One-hundred-sixty-six heactivesexually active women volunteers were recruited in four centers and randomly assigned for 6 months to either placebo ring use or control (non-use) using a predetermined randomization code generated by WHO in a 2 1 ratio.
Similar(57)
Each quality objective was evaluated using a predetermined standard.
Four equivalent fields were analyzed per gel using a predetermined sampling protocol.
One investigator (CS) selected the articles and collected the data, using a predetermined form.
One investigator (CGV) selected the articles and collected the data using a predetermined form.
Flaking xerotic skin was assessed using a predetermined scale (Table 1).
CIMTs were measured using a predetermined, standardized scanning protocol for the right and left carotid arteries.
Two authors (TAV and MT) independently extracted data using a predetermined template.
Corneal clarity was recorded using a predetermined 5-scale grading of haze [ 19].
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com