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Screening For First Trimester's Hyperglycemia in High and Low Risk Pregnancy

Recruiting
Conditions
Screening for Hyperglycemia in First Trimester in High and Low Risk Pregnancy
Interventions
Diagnostic Test: blood sugar
Registration Number
NCT06064552
Lead Sponsor
Sohag University
Brief Summary

Glucose intolerance is the commonest medical disorder complicating pregnancy. Hyperglycemia increases the risk of delivering a large for gestational age newborn (LGA) and related complications such as operative delivery, birth trauma and the poor adaptation of the newborn . Maternal risks of GDM include also polyhydramnios, preeclampsia, premature delivery, prolonged labor, uterine atony, postpartum hemorrhage, infection and progression of retinopathy which are the leading global causes of maternal morbidity and mortality .Detection of women at higher risk for GDM early in pregnancy is a desirable goal because interventions such as diet, medication, and exercise may be applied earlier in pregnancy and potentially can reduce later development of GDM or its associated morbidities. Most GDM cases are diagnosed after mid-gestation following an abnormal glucose challenge test (GCT). However, about 10% of patients with GDM can be diagnosed in the first trimester.

Detailed Description

Not available

Recruitment & Eligibility

Status
RECRUITING
Sex
Female
Target Recruitment
100
Inclusion Criteria
  • • History of gestational diabetes in previous pregnancies

    • Polycystic ovaries syndrome
    • History of Macrosomic baby in previous pregnancies
    • Past history of late third trimester fetal demise
    • Past history of polyhydramnios
    • Overweight /Obese women Women diagnosed to have other endocrinopathies like suprarenal, thyroid or pituitary disorders Multi fetal pregnancies Past history of shoulder dystocia Past history of preeclampsia Family history of diabetes

In addition, a comparable group of low-risk women will be included like primigravida healthy women or those with normal obstetric history.

Exclusion Criteria
  • all patient not have thev inclusion criteria

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
high risk pregnancyblood sugarPregnant women with history of gestational diabetes in previous pregnancies, Polycystic ovaries syndrome, history of Macrosomic baby in previous pregnancies, Past history of late third trimester fetal demise, Past history of polyhydramnios, Overweight /Obese women, Women diagnosed to have other endocrinopathies like suprarenal, thyroid or pituitary disorders, multi fetal pregnancies, Past history of shoulder dystocia, Past history of preeclampsia
low risk pregnancyblood sugaraverage risk population like primigravida healthy women or those with normal obstetric history.
Primary Outcome Measures
NameTimeMethod
blood sugar percentage1 year

High and low risk women will undergo measuring fasting blood sugar after fasting 6-8hours with good hydration. then measuring blood sugar 1hrs and 2hrs postprandial. for patient with high results (FBS\>95mg/dl, 1hr postprandial\>126mg/dl, 2hrs postprandial \>140mg/dl)

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Sohag university Hospital

🇪🇬

Sohag, Egypt

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