The Role of Umbilical Cord Thickness in Prediction of Fetal Macrosomia in Patients With Gestational Diabetes Mellitus

July 11, 2016 updated by: Rehab Mohamed Abdelrahman, Ain Shams University

The Role of Umbilical Cord Thickness, Interventricular Septum Thickness and HbA1C Levels in Prediction of Fetal Macrosomia in Patients With Gestational Diabetes Mellitus

The aim of this work is the prediction of fetal macrosomia by measuring:

  1. HbA1C.
  2. Umbilical cord thickness.
  3. Interventricular septum thickness.

Study Overview

Status

Completed

Detailed Description

This prospective case control study will be carried out at Ain shams university maternity hospital between April 2015 and October 2015 on 80 patients. The patients will be divided into two groups, 40 pregnant women as case group with gestational diabetes mellitus and 40 non diabetic pregnant women as control group after being approved by the local hospital ethics and research committee. A verbal consent will be taken from each patient.

The following investigation will be performed:

  1. Calculation of gestational age will be based on the last reliable menstrual period or ultrasound examination within the first trimester.

    The ultrasound examination will be with Voluson E6 equipped with a 3.5 Hz trans-abdominal probe at fetal medicine unit of maternity hospital Ain Shams University.

  2. Ultrasound examination will be performed twice at 27-28 weeks and 36-37 weeks of gestation prospectively.

    During ultrasound, fetal biometry (biparietal diameter, abdominal circumference, femur length) and estimated fetal weight will be calculated automatically according to hadlock's formula additionally, the sonographic cross sectional area of umbilical cord, the umbilical arteries and umbilical vein will be measured in a free loop of the umbilical cord using the software of the ultrasound device.

    The cross sectional area of Wharton's jelly will be computed by subtracting the cross sectional area of the vessels from that of the umbilical cord and the interventricular septum thickness will be measured.

  3. HbA1c levels will be measured for diabetes patients.

All the patients will be subjected to :

  1. Full history taking including last menstrual period, medical history and past obstetric history.
  2. Detailed general physical history examination and obstetrics examination.
  3. Ultrasound examination in fetal medicine unit maternity hospital Ain shams university.
  4. Venous blood samples will be taken from patients with gestational diabetes mellitus in clinical pathology department Ain Shams University, to measure the level of HbA1c using immunoassay technique. The patients will be followed up till delivery. The neonates will be weighed and fetal macrosomia will be diagnosed if fetal weight is 4 kg or more.

Study Type

Observational

Enrollment (Actual)

80

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

20 years to 35 years (Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

Female

Sampling Method

Non-Probability Sample

Study Population

This prospective case control study will be carried out at Ain shams university maternity hospital between April 2015 and October 2015 on 80 patients. The patients will be divided into two groups, 40 pregnant women as case group with gestational diabetes mellitus and 40 non diabetic pregnant women as control group after being approved by the local hospital ethics and research committee. A verbal consent will be taken from each patient.

Description

Inclusion Criteria:

  1. Singleton gestation.
  2. Gestational age over 27 weeks.
  3. Intact membranes.
  4. Normal umbilical morphology (two arteries and one vein).
  5. Diagnosis of gestational diabetes.

Exclusion Criteria:

  1. The presence of fetal congenital anomalies.
  2. Multifetal pregnancy.
  3. Maternal chronic diseases (hypertension, renal disease, cardiac and pulmonary disease, etc.).
  4. Patients with a diagnosis such as oligohydramnios , pre-eclampsia and intrauterine growth retardation.
  5. Patients who used cigarettes or alcohol during pregnancy.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
pregnant women with gestational diabetes
case group
non diabetic pregnant women
control group

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
The Number of Participants Who Were Diagnosed With Fetal Macrosomia (Birth Weight)
Time Frame: at birth
The neonates will be weighed and fetal macrosomia will be diagnosed if fetal weight is 4 kg or more.
at birth

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Umbilical Cordcross-sectional Area
Time Frame: 36-37 weeks of gestation
the sonographic cross sectional area of umbilical cord, the umbilical arteries and umbilical vein will be measured in a free loop of the umbilical cord using the software of the ultrasound device.
36-37 weeks of gestation
Prediction of Fetal Macrosomia by Measuring HbA1C in Participants
Time Frame: 36-37 weeks of gestation
Venous blood samples will be taken from participants in clinical pathology department Ain Shams University, to measure the level of HbA1c using immunoassay technique.
36-37 weeks of gestation
Interventricular Septum Thickness
Time Frame: 36-37 weeks of gestation
The interventricular septum thickness will be measured by ultrasound examination
36-37 weeks of gestation

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

April 1, 2015

Primary Completion (Actual)

October 1, 2015

Study Completion (Actual)

November 1, 2015

Study Registration Dates

First Submitted

December 26, 2015

First Submitted That Met QC Criteria

December 29, 2015

First Posted (Estimate)

December 31, 2015

Study Record Updates

Last Update Posted (Estimate)

August 18, 2016

Last Update Submitted That Met QC Criteria

July 11, 2016

Last Verified

July 1, 2016

More Information

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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