Actively Recruiting

Age: 18Years - 40Years
FEMALE
Healthy Volunteers
NCT07336173

Uterine Artery Doppler Indices and Uterocervical Angle Measurment in Prediction of Preterm Labor

Led by Kafrelsheikh University · Updated on 2026-01-20

47

Participants Needed

1

Research Sites

19 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The goal of this observational study is to evaluate the role of uterine artery doppler indices and uterocervical angle measurement in prediction of preterm labor .The main question it aims to answer is: Does combination of both uterine artery doppler indices and uterocervical angle measurement increase sensitivity and specificity for prediction of established preterm labor ? Participants already performing uterine artery doppler as part of their regular antenatal care .measurement of anterior uterocervical angle will be added between 24 to 34 weeks gestation to predict preterm labor in candidates .

CONDITIONS

Official Title

Uterine Artery Doppler Indices and Uterocervical Angle Measurment in Prediction of Preterm Labor

Who Can Participate

Age: 18Years - 40Years
FEMALE
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients who give verbal and written informed consent
  • Pregnant women aged 18 to 40 years
  • Singleton pregnancy
  • Gestational age confirmed by first trimester ultrasound scan before 14 weeks
  • Gestational age between 24 and 34 weeks
  • Threatened preterm labor defined as at least one uterine contraction every 10 minutes lasting 30 seconds or more, cervical dilation 3 cm or less, and cervical effacement less than 80%
Not Eligible

You will not qualify if you...

  • Ruptured membranes
  • Clinical signs of chorioamnionitis
  • Fetal compromise on evaluation
  • Severe obstetric complications such as severe preeclampsia or eclampsia
  • Diagnosed intrauterine growth restriction (IUGR)
  • Congenital fetal anomalies
  • Multiple pregnancies
  • Previous cervical surgery like cone biopsy or cerclage
  • Significant maternal medical disorders such as chronic hypertension, diabetes mellitus, or liver dysfunction
  • Severe non-obstetric complications like acute abdomen

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Kafr elsheikh university hospital

Kafr ash Shaykh, Egypt

Actively Recruiting

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Research Team

N

Nourhan M Shalaby, Master

CONTACT

A

Ahmed M Fathy, MD

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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