Study ID | |
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Type of study | RCT Quasi‐RCT Non‐ RCT |
Comments on study design | |
Does the study compare the use BIS (BIS group) and the use of clinical signs (SP group) in guiding doses of anaesthetics? | |
Was the assignment of subjects to treatment groups randomized? | |
Was there blinding? If so, who was blinded | Subject ‐Blinded? Yes/No/Unclear Anaesthesiologist Blinded? Yes/No/Unclear Outcome accessor blinded? Yes/No/Unclear |
Were the BIS and SP groups similar at the start of the trial? | |
Apart from the treatment under investigation, were the groups treated equally? | |
Are all relevant outcomes measured in a standard, valid and reliable way? | |
What percentage of the individuals or clusters recruited into the study are included in the analysis? | |
Were all the subjects analysed in the groups to which they were randomly allocated? |