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Clinical Trial Summary

The design of the study is post-marketing, observational, multi-centre and open-label. The study does not provide treatment; only patients to whom misoprostol 200 µg vaginal delivery system (VDS) is prescribed may be included. All directions for medication usage and patient monitoring are solely at the discretion of the investigator in accordance with their usual practice and must be consistent with the Dutch prescribing information of misoprostol 200 µg VDS. No other (invasive) study-related interventions or measurements are done, other than the procedures routinely performed during induction of labour. No effort is expected from the study subjects. 150 patients from 20 Dutch centres will be included.


Clinical Trial Description

n/a


Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


NCT number NCT02242214
Study type Observational [Patient Registry]
Source Ferring Pharmaceuticals
Contact
Status Completed
Phase N/A
Start date September 2014
Completion date August 2015

See also
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Terminated NCT02932319 - Outpatient Foley Catheter for Induction of Labor in Nulliparous for Prolonged Pregnancy N/A
Not yet recruiting NCT04743297 - Propess Versus Prostin for Induction of Labour in Women With Term PROM Phase 4
Not yet recruiting NCT04887493 - To Study the Efficacy and Safety of Misoprostol by Sublingual Routes for Induction of Labour N/A
Completed NCT04454346 - Double Foley Catheter For Cervical Ripening N/A
Completed NCT00299754 - Trial Of Misoprostol And Dinoprostone Vaginal Pessaries for Cervical Priming (TROMAD Study) Phase 3
Completed NCT04477226 - Transvaginal Ultrasound As Predictors of Successful Induction of Labour
Completed NCT03355040 - Induction of Labour for LGA fœtus in Women Without Insulin-treated Diabetes.
Completed NCT03489928 - Misoprostol Labour Induction Study Phase 3