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Comparison Between Ultrasonographic Cervical Length and Bishop Score in Preinduction Cervical Assessment

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01317706
Enrollment
154
Registered
2011-03-17
Start date
2008-11-30
Completion date
2010-08-31
Last updated
2011-03-17

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

Conditions

Failed Induction of Labor

Keywords

Bishop score, Cervical length, Cervical ripening, Labor induction

Brief summary

To compare the ultrasonographic cervical length with the Bishop score in determining the administration of prostaglandin for preinduction cervical ripening in nulliparas at term.

Interventions

Assessment of cervical status based on Bishop score versus sonographically measured cervical length

Sponsors

Seoul National University Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
DIAGNOSTIC
Masking
DOUBLE (Subject, Caregiver)

Eligibility

Sex/Gender
FEMALE
Healthy volunteers
No

Inclusion criteria

* nulliparous patients * singleton pregnancy * live fetus with vertex presentation * intact amniotic membranes * \> 37 weeks gestation * absence of labor * no previous uterine surgical procedures

Exclusion criteria

* major congenital anomaly

Design outcomes

Primary

MeasureTime frameDescription
Successful labor inductionEleven hours of initiating oxytocin on the fist day of inductionInduction success was defined as an ability to achieve the active phase of labor corresponding to a cervical dilatation of ≥ 4 cm within 11 hours of initiating oxytocin (i.e., within 22 hours of the administration of a dinoprostone vaginal insert) on the first day of induction.

Secondary

MeasureTime frameDescription
the need for oxytocin inductionAfter removing prostaglandin, the following day when an intravenous oxytocin infusion was started1. the interval from start of oxytocin to the active phase of labor 2. the interval from start of oxytocin to delivery 3. vaginal delivery within 24 hours of starting induction 4. the incidence of cesarean delivery

Countries

South Korea

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026