N/A
N=200
Cervical Length and Bishop Score in Preinduction Cervical Assessment Prior to Induction of Labor
Cervical Dystocia
Bottom Line
View on ClinicalTrials.gov: NCT02694315 ↗Enrolled (actual)
200
Serious AEs
0.0%
Results posted
Nov 2016
Primary outcome: Primary: Cervical Length Prior to Labor Induction — 2.9; 3 centimetres
Study Design & Population
- Study type
- Observational
- Phase
- N/A
- Interventions
- Bishop score (Other); cervical length (Other)
- Age
- Pediatric, Adult · 17+ yrs
- Sex
- Female
- Sponsor
- Ain Shams Maternity Hospital
- Primary completion
- Mar 2016
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Cervical Length Prior to Labor Induction |
2.9; 3 | — |
| PRIMARY Bishop Score Prior to Induction of Labor |
4; 3 | — |
Summary
Comparison between Sonographic Cervical Length and Bishop Score in Preinduction Cervical Assessment prior to induction of labor as regards induction success.
Eligibility Criteria
Inclusion Criteria
- Nulliparous patients.
- Singleton pregnancy.
- Living fetus with cephalic presentation.
- Absence of labor pain.
- Gestational age 37-42 weeks.
- No previous uterine surgical procedures.
- No Liquor abnormalities.
- Fetal weight less than 4 kilograms.
Exclusion Criteria
- Non-vertex presentation.
- Previous uterine surgery.
- Multiple pregnancy.
- Fetal or maternal complications that might cause cesarean section.
- Liquor abnormalities.
- Fetal weight more than 4 kilograms.
- Abnormal umbilical artery Doppler indices or non-stress test.
- Asthmatic patients or women with allergy to prostaglandins.
Data sourced from ClinicalTrials.gov (NCT02694315). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.