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Future trials should consider examining adjuvant treatment escalation in patients with >5 lymph nodes.
Future trials should consider standardizing the amount of available glycemic carbohydrate in study meals that assess the effect of 'catalytic' doses of fructose from whole foods.
Future trials should consider acute and extended use of novel agents to better match the pathophysiology of decompensation and recovery from acute HF.
Future trials should consider screening for depression before recruiting patients.
Future trials should consider a number of crucial variables, including dose.
Future trials should consider the use of composite end points that also include relevant safety end points.
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The design of future vaccine trials should consider diverse regional epidemiological scenarios.
The design of future vaccine trials should consider the diverse regional epidemiological scenarios regarding naive and immune population.
46 47 Therefore, future clinical trials should consider provision of problem led, benign, and parsimonious interventions that target presenting difficulties (be they anxiety disorders, depression, or distressing attenuated psychotic experiences) rather than prevention of transition to first episode psychosis in itself.
Future randomized controlled trials should consider the dose of ethanol and the duration of ethanol consumption and abstention in the experimental design.
However, considering its apparent prognostic value, future randomised controlled trials should consider reporting median CA19-9 levels in treatment groups as part of routine demographic data.
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