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

NCT ID: NCT02643225

Last Updated: 2016-08-18

Basic Information

• Recruitment Status: COMPLETED
• Total Enrollment: 80 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2015-04-30
• Study Completion Date: 2015-11-30

Brief Summary

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

1. HbA1C.

2. Umbilical cord thickness.

3. Interventricular septum thickness.

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.

Conditions

Gestational Diabetes

Study Design

• Observational Model Type: CASE_CONTROL
• Study Time Perspective: PROSPECTIVE

Study Groups

pregnant women with gestational diabetes

case group

No interventions assigned to this group

non diabetic pregnant women

control group

No interventions assigned to this group

Eligibility Criteria

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.

• Minimum Eligible Age: 20 Years
• Maximum Eligible Age: 35 Years
• Eligible Sex: FEMALE
• Accepts Healthy Volunteers: Yes

Sponsors

Ain Shams University

OTHER

Sponsor Role: lead

Responsible Party

Rehab Mohamed Abdelrahman

Lecturer of Obstetrics and Gynaecology Faculty of Medicine, Ain Shams University

Responsibility Role: PRINCIPAL_INVESTIGATOR

Other Identifiers

Diabetes mellitus

Identifier Type: -

Identifier Source: org_study_id