Bishop Score vs. Cervical Length in Labor Induction

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
AgeNot listed
SponsorAssiut University

About this trial

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

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Singleton pregnancy

Disqualifiers

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

Trial population

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.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

88 Participants
are grouped into 2 trial groups
Group A: Transvaginal Ultrasound Group (TVUS):
Group B: Bishop Score Group (BS):

Trial outcomes

Primary outcomes

1

Rate of vaginal delivery

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

Time frame
Within 24 hours

Secondary outcomes

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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