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. 2001 Apr 23;2001(2):CD003098. doi: 10.1002/14651858.CD003098

Lange 1981.

Methods Allocation: "random", not further described. 
 Blinding: none described. 
 Study period: not stated.
Participants Inclusion criteria: women with PROM at or near term of at least 6 hours without labor activity and cervix less than 3 cm dilated. 
 Setting: University Hospital, Odense, Denmark. 
 Number of participants: n = 201.
Interventions Oral PGE2 0.5 mg hourly and with increases up to 1.5 mg per hour depending on response (n = 99) vs IV oxytocin up to 45 miliunits per minute (n = 102).
Outcomes Induction to delivery time. 
 Mode of delivery. 
 Apgar score less than 8. 
 Gastrointestinal side‐effects.
Notes The Bishop scores of the oxytocin group were slightly higher overall and there were fewer women with scores of less than 6 (24 vs 28).
Risk of bias
Bias Authors' judgement Support for judgement
Allocation concealment (selection bias) Unclear risk B ‐ Unclear