Cervical Ripening Before Induction of Labour at Term: a Randomised Comparison of Prostin vs Propess

Institut National de la Santé Et de la Recherche Médicale, France

Status and phase: Withdrawn; Phase 3

Conditions: Labor, Induced; Cervical Ripening

Treatments: Drug: Prostaglandin E2

Study type: Interventional

Funder types: Other

Identifiers

NCT00545194

PROPESS Study

Details and patient eligibility

About

The aim of this study is to compare two different preparation

Sex: Female

Ages: 18 to 45 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• singleton pregnancy
• cephalic presentation
• gestation of more than 37 Weeks confirmed by ultrasound
• Bishop score less than 7
• Informed consent

Exclusion criteria

• previous cesarean section (scarred uterus)
• polyhydramnios
• multiple pregnancy
• fetal malformation

Trial design

0 participants in 2 patient groups

A

Active Comparator group

Description:

sustained release preparation of prostaglandin E2

Treatment:

Drug: Prostaglandin E2

B

Active Comparator group

Description:

short-acting (instant-released) preparation of prostaglandin E2

Treatment:

Drug: Prostaglandin E2