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The sizes of the concrete slabs and areas of the bonding zone are the primary studied parameters.
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The primary study endpoint was 90-daysmortality.
The primary study is not direct related to Pentest EC2.
The primary study discusses one or more tools for Pentest.
Two authors independently extracted data from the primary studies.
The primary study endpoints were technical success and safety.
The figures give the age of blood for each study comparing the primary study outcome.
The primary study endpoint was the number of ICU days with SIRS.
These criteria help, as the main objective, to evaluate the reliability of the primary studies.
(3) The correlations among the proxy variables have to be stated in the primary study.
The primary study period was the first two cycles (12 weeks) of treatment.
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