Sentence examples for trials boundaries from inspiring English sources

Exact(1)

In clinical trials boundaries for early stopping after an interim analysis may be incorporated.

Similar(59)

Trial boundaries are rationalised to four values of seasonal performance providing the opportunity to reassess the UK EST heat pump trial results and identify two boundary conditions directly relevant to the interpretation of the Renewable Energy Sources Directive.

The activists said the trial, at Rothamsted Research in Harpenden, Hertforshire, is a threat to agriculture because pollen from the GM wheat could contaminate non-GM plants outside the trial boundary.

A power analysis was conducted using simulations of continuously monitored, trial-stopping boundaries to determine the accrual buffer needed to suspend a trial after an adverse event (7).

Because no reason exists why the standards for a meta-analysis should be less rigorous than those for a single trial, analogous trial sequential monitoring boundaries can be applied to meta-analysis as trial sequential analysis.

Because there is no reason why the standards for a meta-analysis should be less rigorous than those for a single trial, analogous trial sequential monitoring boundaries can be applied to meta-analysis.

Since there was no significant trend in the effects by distance from the trial area boundary (Table 2), extrapolations assumed that effects were consistent throughout the affected areas.

We used previously published methods [10], [11] to investigate whether the effect of culling varied with distance from the trial area boundary.

The sequential analysis confirmed the primary meta-analysis when using the traditional 5% level of statistical significance (figure 3), but not after adjusting for multiple testing (the trial monitoring boundary was not crossed).

Within the president's orbit, people described Trump as furious and "lit up" by the recent developments, and floating a trial balloon to test the boundaries of trying to halt Mueller's burgeoning probe.

In order to calculate the required information size and the cumulative Z-curve's eventual breach of relevant trial sequential monitoring boundaries [17], [18], the trial sequential analysis was based on a type I error of 5%, a beta of 10% (power of 90%), the variance of all the trials (as no trial had low risk of bias), and a minimal relevant difference of 2 points on the HDRS.

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