Foley catheter balloon for cervical ripening in term pregnancy: a multicenter randomized controlled trial

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR-TRC-13003044

Enrollment

Unknown

Registered

2013-01-24

Start date

2013-02-01

Completion date

Unknown

Last updated

2017-04-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

High risk pregnancy

Interventions

A:30ml balloon for 12 hours

B:30ml balloon for 24 hours

C:80ml balloon for 12 hours

D:80ml balloon for 12 hours

Eligibility

Sex/Gender

Female

Age

18 Years to 45 Years

Inclusion criteria

Inclusion criteria: Term gestation (>37 weeks), singleton,cephalic presentation, intact membrane, indicated for induction of labor, cervical Bishop score <6

Exclusion criteria

Exclusion criteria: Maternal age< 18, rupture of membranes, multifetal gestation, abnormal pelvic measurement, malpresentation, low-lying placenta, genital tract infection GBS positive

Design outcomes

Primary

Measure	Time frame
vaginal delivery rate within 24 hour;	—

Secondary

Measure	Time frame
cesarean section rate;induction to delivery time interval;rate of failed induction;oxytocin requirement;operative vaginal delivery rate;5-minute Apgar score;NICU admission;Maternal intrapartum infection;	—

Countries

China

Contacts

Public ContactYali Hu

yali_hu@hotmail.com+86 13951846008

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Mar 4, 2026