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Effect of mechanical ripening of the cervix before induction of labor with misoprostol. A randomized multicenter trial.

Randomized multicenter study of mechanical ripening of the cervix by double balloon device (COOK CRB [Cervical Ripening Balloon]) before oral misoprostol (OM) versus OM alone to improve efficacy in inducing labor.

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12611000537954
Enrollment
250
Registered
2011-05-25
Start date
2011-05-15
Completion date
Unknown
Last updated
2020-01-13

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

Conditions

None listed

Brief summary

Induction of labor is a common obstetric procedure that is being more widely used nowadays than ever before. Pharmacologic and mechanical methods are used to induce labor. As there are different modes of action, a reduced induction-to-delivery time can be expected if mechanical and pharmacologic methods are used consecutively. The hypothesis is that mechanical dilation (CRB - a double balloon device) before pharmacological induction (oral misoprostol) improve the efficacy of labor induction. This hypothesis supposed to be checked in a multicenter trial with different misoprostol regimes.

Interventions

A double-balloon catheter for cervical ripening (COOK CRB) is used the first day (for a maximum of 12 hours) before inducing labor with misoprostol the second day. Each participating hospital uses its own misoprostol regime. e.g. the regime of the primary study unit: First day: CRB (for a maximum of 12 hours) Second day: OM 50 microg with repeat doses 4 and 8 hours later if necessary Third day: OM 100 microg with repeat doses 4 and 8 hours later if necessary Fourth day: misoprostol 100 microg

A double-balloon catheter for cervical ripening (COOK CRB) is used the first day (for a maximum of 12 hours) before inducing labor with misoprostol the second day. Each participating hospital uses its own misoprostol regime. e.g. the regime of the primary study unit: First day: CRB (for a maximum of 12 hours) Second day: OM 50 microg with repeat doses 4 and 8 hours later if necessary Third day: OM 100 microg with repeat doses 4 and 8 hours later if necessary Fourth day: misoprostol 100 microg vaginally with repeat doses 4 and 8 hours later if necessary

Sponsors

Sven Kehl
Lead SponsorIndividual

Study design

Allocation
Randomised controlled trial
Primary purpose
Treatment

Eligibility

Sex/Gender
All
Age
18 Years to 45 Years
Healthy volunteers
Yes

Inclusion criteria

singleton pregnancy at term greater than 259 days of gestation, vertex presentation, indication for induction of labor, and an unfavorable cervix (Bishop score < 8)

Exclusion criteria

Premature Rupture of Membranes (PROM), contraindication for labor induction with misoprostol (e.g. placenta previa, previous cesarean sections), cases of structural or chromosomal malformation, intrauterine fetal death.

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026