Randomized controlled trial of Propess versus amniotomy and oxytocin for induction of labour

Dinoprostone vaginal extended release system (Propess) for induction of labour versus amniotomy plus syntocinon, a randomized controlled trial

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR-TRC-14004079

Enrollment

Unknown

Registered

2014-01-03

Start date

2014-02-01

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

Induction of labour

Interventions

two groups:

Eligibility

Sex/Gender

Male

Inclusion criteria

Inclusion criteria: Nulliparous pregnant women admitted to antenatal ward for induction of labour at or more than 37 weeks with favourable cervix according to modified Bishop score (>=6)

Exclusion criteria

Exclusion criteria: Rupture of membranes, women aleready in labour before recruitment, presence of indication for caesarean section, major fetal anomaly, women with unfavourable cervix.

Design outcomes

Primary

Measure	Time frame
Failed induction rat;	—

Secondary

Measure	Time frame
Patient satisfaction score, Total admission time (;	—

Contacts

Public ContactChor Chung Ming

cmchor@cuhk.edu.hk+852 2632 3190

Outcome results

None listed

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