Kass 2001.
Methods | RCT Blinding of randomization ‐ can't tell Blinding of intervention ‐ no Complete follow‐up ‐ yes Blinding of outcome measurement ‐ can't tell | |
Participants | 71 healthy male NB | |
Interventions | lidocaine DPNB (n=24) 2ml D50W orally (n=23) 2 ml H2O orally (n=24) WT 2 to 6 min | |
Outcomes | time cry (primary outcome); HR; O2sat ; modified behavioral pain scale | |
Notes | ‐ additional data obtained from authors ‐ no pacifiers used ‐ Gomco clamp | |
Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Allocation concealment? | Unclear risk | B ‐ Unclear |