CompletedNot Applicable

Clinical Evaluation of Cervical Ripening in the Outpatient Setting

Portugal101 participantsStarted 2020-01-15

Plain-language summary

A randomized controlled trial of mifepristone 200mg vs balloon catheter for cervical ripening.

Who can participate

Age range18 Years – 45 Years

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: * Pregnant woman scheduled for induction of labor. * Age between 18 and 45 years. * Understanding and capable to sign informed consent. * Singleton pregnancy. * Gestational age ≥ 37 0/7 weeks. * Live fetus in cephalic presentation. * Intact membranes * Bishop score \< 6 * Estimated fetal weight \< 4500g * Without contraindication to vaginal delivery * No major fetal anomaly Exclusion Criteria: * Previous cesarean section or myomectomy * Hypertension * Diabetes * Thyroid disease * Maternal conditions with high risk of placental insufficiency

What they're measuring

Number of Participants with Bishop score ≥6 or spontaneous labour

Timeframe: 24 hours

Trial details

NCT IDNCT04271722

SponsorCentro Hospitalar Lisboa Norte

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2022-12-30

View on ClinicalTrials.gov More Labor; Forced or Induced, Affecting Fetus or Newborn trials