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Objective
To assess adverse event (AE) resolution, delivery mode and neonatal outcomes after misoprostol or dinoprostone vaginal insert (MVI or DVI) retrieval due to AE during induction of labour (IOL).
Design
Randomised, double‐blind trial, EXPEDITE.
Setting
Thirty five obstetric departments, USA.
Population
Consisted of 1358 pregnant women with modified Bishop score ≤4 eligible for pharmacological...