| Methods |
|
| Participants |
|
| Interventions |
|
| Outcomes |
|
| Notes |
See Table 8
|
| Risk of bias |
| Bias |
Authors' judgement |
Support for judgement |
| Random sequence generation (selection bias) |
Low risk |
"Randomization [...] by drawing lots" |
| Allocation concealment (selection bias) |
Unclear risk |
Not described. |
| Blinding (performance bias and detection bias)
Subjective outcomes |
High risk |
Participants aware of group allocation. |
| Blinding (performance bias and detection bias)
Objective outcomes |
High risk |
RR measured via observation (not blind). BP measure via bedside cardiac monitor (automated). |
| Incomplete outcome data (attrition bias)
All outcomes |
Unclear risk |
Withdrawals and drop‐outs not described. |
| Selective reporting (reporting bias) |
Unclear risk |
Not known. |
| Protection from contamination? |
High risk |
Cross‐over design. |
