Basnet 2010.
Methods | RCT Painful intervention: venipuncture Study location: Neonatal ward of Tribhuvan University Teaching Hospital, Kathmandu, Nepal Study period: February to August 2006 |
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Participants | 50 term infants aged between 12 h to 8 days Mean post‐natal age: 59.92 h no treatment group; 68.76 h sucrose group |
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Interventions | No treatment group (n = 25) Sucrose group (n = 25): received 2 ml of 30% sucrose orally 2 minutes before venipuncture |
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Outcomes | DAN score, duration of cry, number of infants crying | |
Notes | Data for DAN scores were reported as median and IQRs. Duration of cry was reported as mean and SD and was included in meta‐analyses | |
Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Low risk | Used random numbers from 1 to 50 developed from a random number table |
Allocation concealment (selection bias) | High risk | Authors did not report whether the opaque, sealed envelopes used to allocate participants were sequentially numbered |
Blinding (performance bias and detection bias) All outcomes | Low risk | Personnel blinded |
Blinding of outcome assessment (detection bias) All outcomes | Low risk | Outcome assessors blinded |
Incomplete outcome data (attrition bias) All outcomes | Low risk | Outcome reported for all randomized infants |
Selective reporting (reporting bias) | Unclear risk | One rating scale (DAN) listed in methods section and is reported in results table. The study protocol was not available to us so we could not judge whether there were any deviations from it |
Other bias | Low risk | Appears free of other bias |