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Alternatively, in order to establish assay sensitivity using a non-inferiority trial design, it could be useful to include a placebo group in addition to the active control group [ 32].
However, in some contexts it proves useful to include a second stage that simulates the realization of a specific outcome in order to help the user better understand the nature of probabilities.
In such cases, it will be useful to include a subscript indicating the relevant time.
Here, it would be useful to include a systematic assessment of the recommendations' possible effectiveness.
As a next step, it would be useful to include a normalisation of the size of a research group.
In Fig 2 it would be useful to include a representative image of an S3ED-treated aortic ring.
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It is useful to include an appropriate reference if there is evidence in the literature for a particular treatment (e.g. low-dose sulfonylureas in HNF1A/4A MODY) associated with the genetic diagnosis.
It would be useful to include an analysis of randomised trials performed in the appropriate patient groups which have used any comparator and consider them for indirect comparisons with topotecan and, if the data allow, possibly as a network meta-analysis[ 11].
These 'weighted' loadings form the basis of an idea for which indicator would be useful to include in a frailty measure.
The ability of antibodies raised against the functional domain of PfRH2a/b to inhibit erythrocyte invasion suggests that it may be useful to include rPfRH240 in a blood-stage vaccine against P. falciparum malaria.
It would be useful to include more systematically a generic utility instrument to measure QoL in trials.
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