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You can access this
clinical trial
if you have
Labour Induction
and you are
over 18
years old
This is an observational trial.
You are contributing to medical knowledge about your condition.
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The purpose

Objective: To compare the efficacy and safety of the misoprostol vaginal insert (MVI) with an off-label use of oral misoprostol (OM). Design: Pair-matched case-control study. Setting: Tertiary-care academic centre in Germany. Population: A cohort of 138 women ≥ 37/0 weeks pregnant undergoing labour induction. Methods: The induction of labour with a retrievable prostaglandin vaginal insert in a consecutive series of 69 women was compared with induction using oral misoprostol in a pair-matched cohort. Main outcome measures: The primary outcomes were the time from induction to delivery and the caesarean section rate. Secondary outcomes included uterine tachysystole, tocolysis, fetal scalp blood testing, meconium-stained amniotic fluid, umbilical arterial pH, and Apgar score.

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Tris trial is registered with FDA with number: NCT02904317. The sponsor of the trial is Asklepios Kliniken Hamburg GmbH and it is looking for 138 volunteers for the current phase.
Official trial title:
The Misoprostol Vaginal Insert Compared With Oral Misoprostol for Labour Induction in Term Pregnancies: a Pair-matched Case-control Study