Sentence examples for structure of trials from inspiring English sources

Exact(1)

He believes that the real issues are far broader, and include the adversarial structure of trials, confirmation bias, cultural notions about what indicates guilt, and a basic human tendency to attribute meaning to details that may be coincidental.

Similar(59)

There were no significant differences in the preference structure of trial participants, compared to clinic women, or across women who were 1) randomised to, or 2) received the different trial arms, so all 362 respondents were included in the analysis [ 16].

The very structure of clinical trials may be contributing to this because assumptions made during trial planning preclude additional learning within residual important areas of uncertainty, such as dose, timing, and duration of treatment.

The most likely common problem is bias — built into the very structure of these trials.

The group structure of such trials has to be taken into consideration in the analysis and has an impact on the power of the trial.

(A ) Structure of individual trials.

The structure of clinical trials and the process of randomisation are explained in an easy to follow format.

However, if these trials suggest a favourable efficacy and toxicity, the public will be further motivated to directly fund these efforts and national cancer organisations like the NCI, might be inspired to directly contribute to the design and structure of larger trials.

Empirical distributions of the slope of the relationship between proportion paternity and each of the fixed effects in our minimal adequate models were created by shuffling randomly the paternities of fish within tanks, while maintaining the tank structure of the trials.

The supplement will begin with "reminiscences from the early days," providing an historical overview of the letrozole development program by scientists involved in the discovery of letrozole in the laboratory, and the clinicians and statisticians who devised the structure of the trials.

6) discussions on post marketing responsibilities which could include price-volume and binding health outcome agreements between regulators and industry, as well as the appropriate structure of vigilance trials, adverse incident reporting, impact of fraud, prescribing habits and alternative or complementary therapies.

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