Actively Recruiting

Age: 20Years - 35Years
FEMALE
Healthy Volunteers
NCT06644911

Obesity Doppler in Term Pregnancy

Led by Assiut University · Updated on 2025-01-28

240

Participants Needed

1

Research Sites

49 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Maternal obesity is an epidemic in the developed world like Egypt. There are many pregnancy-associated complications including pre-eclampsia, gestational diabetes, and increased rates of septic wound after cesarean delivery. As a potential explanation of the etiology of complications due to maternal obesity, the role of endothelial dysfunction in the systemic and peripheral vasculatures has been hypothesized. It has been proposed that some adverse pregnancy outcomes in obese patients may be mediated by placental insufficiency. Utero-placental insufficiency is typically associated with fetal growth restriction and low birth weight. Umbilical and uterine artery Doppler is widely accepted as a useful tool for monitoring high-risk pregnancies. Normally, uterine artery vascular impedance gradually decreases until the late mid-trimester, owing to the establishment of a low-resistance placental circulation. Obesity has little impact on uterine vascular changes reflected by the early uterine artery PI. However, in the second trimester, extreme obesity appears to impair the normal continued drop in uterine vascular resistance. Many studies have examined the relationship between BMI and Doppler changes in high-risk pregnancies, but few have addressed these changes in low-risk pregnancies.

CONDITIONS

Official Title

Obesity Doppler in Term Pregnancy

Who Can Participate

Age: 20Years - 35Years
FEMALE
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Singleton pregnancy
  • Gestational age 37 weeks or more
  • No fetal structural abnormalities
  • No maternal comorbidities or complications
  • Obese women with BMI 30 kg/m2 or higher
  • Normal weight women with BMI between 18.5 and 24.9
Not Eligible

You will not qualify if you...

  • Placenta previa
  • Antepartum hemorrhage
  • Smoking or alcohol use
  • Preeclampsia
  • Diabetes mellitus
  • Need for urgent termination of pregnancy

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

Woman's Health Hospital - Assiut university

Asyut, Egypt, 71111

Actively Recruiting

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Research Team

M

Mohammed Khairy Ali, 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

2

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