One of us searched for published and unpublished trials, examining trial registries, conference proceedings and the bibliographies of any identified trials and relevant reviews (the search strategy is available upon request).
As our key question related to a potential dissociation between detection and localisation, we carefully examined trials on which there seemed to be a dissociation.
A subsequent meta-analysis examined trials comparing β blockers with other blood pressure lowering drugs.
Finally, we did not examine trials using only other quality of life or health survey instruments beyond SF-36.
Thus, we examined trials with correct versus incorrect T2 report in lag 2 across affective T2 contents.
The systematic evaluation of bias or risk of bias remains an essential aspect of evidence synthesis, as it forces reviewers to critically examine trials.
We examined trial spacing during extinction following a human contingency learning task.
We used a fast event-related functional magnetic resonance imaging (fMRI) design to examine trial-to-trial reaction time (RT) adjustments in 30 MA abusers and 30 controls.
We will also examine trial design; ethical, legal, and organizational aspects of clinical research; application of statistical methods; and the integration of these concepts into practice.
