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. 2017 Apr 13;2017(4):CD011989. doi: 10.1002/14651858.CD011989.pub2
Author (Year)  
Study design/Methods RCT, blinding, randomisation, purpose, when and were was the study conducted?, trial identifier
Participant flow  
  Experimental Control
Number of participants assessed for eligibility    
Number of participants randomised    
Number of participants receiving treatment    
Number of participants analysed    
Inclusion criteria    
Exclusion criteria    
Population/Baseline details Experimental Control
Mean age/Median age    
Mean weight/Median weight    
ASA I/II    
Type of delivery (spontaneous delivery/instrumental/caesarean section)    
Week of gestation    
Singleton, twin, multiple pregnancy    
Parity    
Duration of labour (first stage of labour, second stage of labour)    
Interventions    
Outcomes (primary endpoint, dichotomous, continuous)    
Notes sample size, power analysis, concomitant medications, funding