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Comparison of prostaglandin vaginal suppositories and Foley catheter for induction of labor in full-term hypertensive women

Comparison of prostaglandin vaginal suppositories and Foley catheter for induction of labor in full-term hypertensive women

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500102905
Enrollment
Unknown
Registered
2025-05-21
Start date
2024-09-18
Completion date
Unknown
Last updated
2025-05-26

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

Conditions

hypertensive disorders

Interventions

Foley catheter group:None
dinoprostone vaginal insert group:None

Sponsors

The Third Affiliated Hospital of Zhengzhou University
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: 1.Gestational hypertension or mild preeclampsia; 2. Full-term pregnancy; 3. Cervical Bishop score <7; 4. Singleton pregnancy; 5. Cephalic presentation; 6. No history of oxytocin or prostaglandin allergy; 7. Willingness to undergo labor induction.

Exclusion criteria

Exclusion criteria: 1. History of genital malformations and tumors; 2. Severe preeclampsia; 3. History of previous cesarean section or major uterine surgery; 4. Unstable fetal condition; 5. Active infection of the birth canal; 6. Premature rupture of membranes; 7. Multiple pregnancy; 8. Contraindications to delivery (such as cephalopelvic disproportion); 9. Severe insufficiency of heart, liver, or kidney function

Design outcomes

Primary

MeasureTime frame
successful induction of labor vaginal delivery within 24 hours ;successful induction of labor vaginal delivery within 48 hours ;the induction delivery interval following induction of labor;the interval from induction of labor to the onset of labor;

Secondary

MeasureTime frame
Uterine hyperstimulation;fetal heart-rate abnormality;Severe preeclampsia;postpartum hemorrhage;meconium-stained liquor;placental abruption;neonatal asphyxia;uterine rupture;cesarean section;HELLP syndrome;

Countries

China

Contacts

Public ContactChuang Liu

The Third Affiliated Hospital of Zhengzhou University

zzdxdsfsyy_lc@163.com+86 133 9374 1379

Outcome results

None listed

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