Natural Cervical Ripening to Prevent Pharmacological Induction of Labor - a Pilot Study.

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18+
SponsorUniversity of Zurich

About this trial

As of today, around 25% of all vaginal births happen after induction of labor (IOL). The internal guidelines of the University Hospital Zurich currently recommend pregnant women with a non-insulin dependent gestational diabetes an IOL around term. One possibility to prevent an IOL and increase the chance for a spontaneous onset of birth is a ripening of the cervix by alternative methods in an outpatient setting. The primary objective of this study is to evaluate the effect of natural cervical ripening methods on the time interval between 37 weeks (beginning of the intervention) and the onset of spontaneous labor.

Eligibility criteria

Qualifiers

Singleton gestation

Non-insulin dependent, dietetically managed gestational diabetes

Greater than or equal to 34 weeks.

Planned vaginal birth at the University Hospital of Zurich

Disqualifiers

Pregnant women with multiple gestation

Fetal macrosomia >95th percentile

Intrauterine growth restriction <3rd percentile

Already in labor (regular contractions or premature rupture of membranes (PROM)

Trial design

Treatments tested in this trial

  • Membrane sweaping and Breast massage

Treatment groups

74 Participants
are divided into 2 treatment groups

Sponsors and collaborators