Avraham 2012.

Study characteristics
Methods	Prospective, double‐blind, randomised, controlled study
Participants	61 (29 Ibuprofen, 32 placebo) 61 women who underwent first‐trimester termination of pregnancy (29 Ibuprofen, 32 placebo)
Interventions	Women received 600 mg mifepristone orally, followed by 400 μg oral misoprostol 2 days later. They were randomised to receive pre‐emptively 2 tablets of 400 mg ibuprofen orally or a placebo, when taking the misoprostol. The women completed a questionnaire about side effects and pain score and returned for an ultrasound follow‐up examination 10‐14 days after the medical abortion.
Outcomes	Pain score, GI side effects, complete abortion rate
Notes	Trial registration: NCT00997074 (prospective) Dates: October 2009‐October 2010 Funding: not reported Conflicts of Interest: none disclosed Contact attempted to gather missing data – no response