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The primary analysis was based on trials reporting a most important continuous outcome measure in sufficient detail to be included in the meta-analysis.
The fact that our meta-analysis was based on trials that varied in many ways (for example, with respect to pretreatment blood pressure, previous disease, population sample) may be thought to be a limitation, possibly leading to random error obscuring real differences.
The evidence in the Agency for Health Research and Quality and Institute of Medicine reports was based on trials that used unvaccinated control groups (that is, women who did not receive any type of control vaccination), excluding studies that used hepatitis A vaccine or other vaccines as control interventions.
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This assumption was based on trial activity and discussions with implementers about how IPT would be delivered if introduced as part of routine activity.
Average daily insulin dose was based on trial data.
In this study, the determination of the parameters was based on trial and error.
Representation was based on trial recruitment as well as geographical spread and led to the creation of a national portfolio of phase II and III trials.
To be included, meta-analysis should be based on trials in the field of hepatology and published as full papers before 2000.
Our study is based on trials retrieved from an extensive literature search to identify all relevant eligible trials comparing combination of ARB plus ACE inhibitor therapy to ACE inhibitor therapy alone in patients with congestive heart failure.
More exceptionally, all traditional drug delivery methods are based on trials and errors.
All analyses (behavioral and fMRI) are based on trials with correct preference responses.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com