Raghavan 2009.

Methods	random code generated in blocs of 10; sequentially numbered, sealed envelopes
Participants	480 women; </= 63 days gestation. gestational age confirmed by ultrasound if needed; exclusion criteria:ectopic pregnancy, contraindications to study medication, treatment with anticoagulants, lived more than 1 hour away from hospital; study conducted between July 2005 to November 2006 atUniversity hospital Chisinau, Moldova
Interventions	mifepristone 200mg followed 24 hrs later by: group 1: misoprostol 400mcg sublingual group 2: misoprostol 400mcg oral for sublingual: tablet for 30 min under the tongue and swallow rest after; no repeat doses of misoprostol offered
Outcomes	complete abortion, side effects, acceptibility
Notes
Risk of bias
Bias	Authors' judgement	Support for judgement
Allocation concealment (selection bias)	Unclear risk	B‐unclear