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NCT Number: NCT07208552

Bishop Score vs. Cervical Length in Labor Induction

The study population consists of term primigravida women undergoing induction of labor at a tertiary care referral center in Assiut, Egypt.

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Key information

Sex eligibility

All sexes

Study type

Observational

About this study

Participants include 88 primigravida women at ≥37 weeks of gestation, each with a singleton pregnancy in cephalic presentation. All participants present with medical or obstetric indications for induction of labor, such as post-dates, oligohydramnios, mild preeclampsia, or premature rupture of membranes. Exclusion criteria include prior uterine surgery, multiple pregnancies, malpresentation, placenta previa, vasa previa, non-reassuring fetal status at admission, or maternal infections such as active genital herpes and HIV. A carefully designed sample size calculation ensures adequate power, with a final cohort of 44 women per study arm.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Singleton pregnancy

Cephalic fetal presentation

Gestational age ≥37 weeks (confirmed by reliable dating)

Indication for induction of labor (postdate pregnancy, oligohydramnios, mild preeclampsia, premature rupture of membranes)

Exclusion criteria

  • Previous uterine surgery (e.g., cesarean section, myomectomy)

Multiple gestation

Malpresentation

Placenta previa or vasa previa

Non-reassuring fetal heart status at admission

Active genital herpes or HIV infection

Treatment and study plan

Primary outcomes

  1. Rate of vaginal delivery

    Time frame: Within 24 hours

    The proportion of women achieving vaginal delivery after induction of labor within 24 hours of initiation.

Sponsors and collaborators

Lead sponsor

Assiut University

Other

Registry information

Official study title

Bishop Score Versus Cervical Length by Transvaginal Ultrasound for Predicting Success of Labor Induction Among Primigravida

Important dates

Study start
2026
Primary completion
2027
Study completion
2027
First posted
Oct 6, 2025
Registry last updated
Oct 6, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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