Cervical Length Pre-induction as a Tool to Predict Vaginal Birth

S

Saint Thomas Hospital (HST)

Status

Completed

Conditions

Pregnancy, Prolonged
Cervical Length Measurement

Treatments

Procedure: Cervical length measurement

Study type

Observational

Funder types

Other

Identifiers

NCT02916082
2015-288V2

Details and patient eligibility

About

To evaluate the value of measuring cervical length as a predictor of vaginal birth after induction of labor with prostaglandins in pregnancies with 41 weeks of gestation.

Enrollment

200 patients

Sex

Female

Volunteers

No Healthy Volunteers

Inclusion criteria

  • 41 weeks or more of gestational age
  • Cervical length measured by a FMF certified physician

Exclusion criteria

Any condition that could interfere with a possible vaginal birth (previous cesarean section, hypertensive disorders of pregnancies).

Trial design

200 participants in 1 patient group

Prolonged pregnancy
Description:
Pregnancies with 41 weeks or more of gestation determined by a reliable last menstrual period or early fetal ultrasound.
Treatment:
Procedure: Cervical length measurement

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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