Methods |
"Randomly divided". |
Participants |
10 women recruited from 8 weeks to 'term'. |
Interventions |
CSII versus MDI. |
Outcomes |
Gestational age at birth, caesarean section, weight gain during pregnancy, preterm birth, hyperbilirubinaemia, and maternal days hospitalised. |
Notes |
Single‐centre trial in Italy. |
Risk of bias |
Bias |
Authors' judgement |
Support for judgement |
Random sequence generation (selection bias) |
Unclear risk |
Not reported. |
Allocation concealment (selection bias) |
Unclear risk |
Not reported. |
Blinding of participants and personnel (performance bias)
All outcomes |
High risk |
Blinding of the type of intervention from clinician and participant for the trials was not possible because of the nature of the study. |
Blinding of outcome assessment (detection bias)
All outcomes |
Unclear risk |
Blinding of assessors not reported. |
Incomplete outcome data (attrition bias)
All outcomes |
Unclear risk |
Not reported. |
Selective reporting (reporting bias) |
Unclear risk |
Pre‐specified outcomes not reported. |
Other bias |
Unclear risk |
Small trial group, limited reporting. |