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

Lister 2005

Methods Random allocation ‐ blocked and stratified by physician office and by day of recruitment ‐ day of diagnosis, or after day of diagnosis.
Participants 34 women in Columbus, Ohio, USA, with early pregnancy failure (anembryonic pregnancies or early fetal deaths) diagnosed by TVS.
Interventions Vaginal misoprostol 800 mcg, repeated after 24 hours if sac still present on TVS (n = 18) or placebo (n = 16).
Outcomes Primary: miscarriage complete at 48 hours.
Notes Planned sample size 84 but trial stopped after interim analysis of first 36 women. Two women excluded from analysis ‐ one protocol violation; one did not meet entry criteria. Two women did not come for assessment 2 weeks after initial treatment.
Risk of bias
Bias Authors' judgement Support for judgement
Allocation concealment (selection bias) Low risk A ‐ Adequate