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. 2006 Jul 19;2006(3):CD002253. doi: 10.1002/14651858.CD002253.pub3

Herabutya 1997

Methods "Random allocation" but method not discussed in paper.
Participants 84 women with ultrasound confirmation of fetal death with uterine size < 14 weeks, no bleeding, and cervix closed.
Interventions Misoprostol (200 micrograms vaginally) (n = 42) or vaginal placebo (n = 42) on admission to hospital.
Outcomes Primary outcome was miscarriage within 24 hours of treatment. Some information available on complications.
Notes Much of the outcome data reported describes only the subgroups who did miscarry before surgical evacuation.
Risk of bias
Bias Authors' judgement Support for judgement
Allocation concealment (selection bias) Unclear risk B ‐ Unclear