CompletedPhase 4

Induction of Labor in Term Pregnancies With Unfavourable Cervix

Croatia212 participantsStarted 2018-12-10

Plain-language summary

This is a prospective randomized trial comparing two prostaglandin E2 (dinoprostone) agents used for labor induction in pregnant women with term pregnancies and unfavorable cervix.

Who can participate

SexFEMALE

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * term pregnancies (\> 37 weeks gestation) * unfavourable cervix (Bishop score \<6) * indication for labor induction * absence of uterine contractions * reassuring cardiotocography Exclusion Criteria: * ruptured membranes * scar uterus (previous caesarean section or uterus surgery) * pregnancy complications: intrauterine growth restriction; oligohydramnios, pre-eclampsia, non-reassuring/pathological cardiotocography, cholestasis in pregnancy, diabetes mellitus, multifetal pregnancy, breech presentation

What they're measuring

time period between beginning of labor induction to delivery

Timeframe: 5 days

Trial details

NCT IDNCT04280874

SponsorClinical Hospital Merkur

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2020-07-01

View on ClinicalTrials.gov More Induction of Labor Affected Fetus / Newborn trials