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

Status: Recruiting
Location: See location...
Intervention Type: Procedure
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

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
Participation Requirements
Sex: Female
Minimum Age: 18
Healthy Volunteers: f
View:

• 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

• Planned IOL for 40 weeks of gestation.

• Communication in German and/or English language possible.

Locations
Other Locations
Switzerland
University Hospital Zurich
RECRUITING
Zurich
Contact Information
Primary
Verena Bossung, PD Dr. med.
verena.bossung@usz.ch
+44 43 253 28 47
Backup
Nicole Ochsenbein, Prof. Dr. med
Nicole.Ochsenbein@usz.ch
+41 43 255 51 01
Time Frame
Start Date: 2026-04-10
Estimated Completion Date: 2029-12-31
Participants
Target number of participants: 74
Treatments
Experimental: Study Intervention
Membrane sweeping twice weekly plus intensified breast massage in addition to colostrum banking
No_intervention: Control arm
Standard of care treatment including colostrum banking
Sponsors
Leads: University of Zurich

This content was sourced from clinicaltrials.gov