This, of course, includes visualizing data, checking for outliers, performing spot checks of data, etc. Even in cases where the trial registration number is published as an abstract, this does not guarantee that there will be a one-to-one correspondence between publications and research records, as there are often secondary publications. Clinical trials are also often registered in more than one registry. When multiple ‘screen scans’ are collected, it results in a lot of meaningful information at your fingertips. PRISMA does not require disclosure of the decision procedure for matching trial registry entries with other registries or publications. However, there is currently no requirement to report data integrity checks in the PRISMA checklist. Additional records are created only if new unique data is loaded after the conversion. If the cordon existed, any debris from a crashed spaceship, they would intercept it (“Cordon” works in both directions, as can be seen in the description) and/or possibly have it escorted directly to base. There are some data points in clinical trial records that are presented as machine-readable and were never intended to be interpreted solely by machines. The assumption was that no one would load these data points into a computer program without being read by a human who knew not to read that number as a true estimate of trial participation.
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