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The Effect of Loading Dose of Magnesium Sulfate on Uterine, Umbilical, and Fetal Middle Cerebral Arteries Doppler, Biophysical Profile, CTG, Maternal Vital Signs in Women With Severe Preeclampsia

Cairo University (CU) logo

Cairo University (CU)

Status

Unknown

Conditions

Preeclampsia

Treatments

Drug: MgSO4

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

100 women with severe preeclanpsia received Magnesium sulfate 6 grams intravenous over 20 minutes as a loading dose. Resistance index [RI], pulsatility index [PI] and systolic/diastolic [S/D] ratio of the umbilical artery, uterine aryery and fetal middle cerebral artery before and repeated 20 minutes after intravenous administration of 6 grams of magnesium sulphate (loading dose) over 20 minutes . fetal breathing movements and fetal gross movements are counted within 20 minutes, before and after intravenous administration of 6 grams of magnesium sulphate (loading dose) over 20 minutes

Full description

100 women with severe preeclanpsia received Magnesium sulfate 6 grams intravenous over 20 minutes as a loading dose. Resistance index [RI], pulsatility index [PI] and systolic/diastolic [S/D] ratio of the umbilical artery, uterine aryery and fetal middle cerebral artery before and repeated 20 minutes after intravenous administration of 6 grams of magnesium sulphate (loading dose) over 20 minutes . fetal breathing movements and fetal gross movements are counted within 20 minutes, before and after intravenous administration of 6 grams of magnesium sulphate (loading dose) over 20 minutes

Enrollment

100 estimated patients

Sex

Female

Ages

20 to 40 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Singleton pregnancy.

  • Primigravida or Multigravida.

  • Pregnant females ≥ 37 weeks of gestation.

  • Diagnosed as severe preeclampsia by the following criteria:

    • Sustained systolic blood pressure of ≥160 mmHg or a sustained diastolic blood pressure of ≥ 110 mmHg.
    • Proteinuria measured as +1 or more by dipstick or 24 hours urine collection with proteinuria ≥ 0.3 grams.
    • Oliguria or creatinine > 1.1 mg%.
    • Laboratory findings characteristic of HELLP syndrome.
    • Symptoms suggestive of severe preeclampsia ; severe headache, blurring of vision, epigastric pain.

Exclusion criteria

  • Multifetal pregnancy.
  • History of epilepsy.
  • Patients with diabetes.
  • Patients with renal disease.
  • Fetuses with congenital anomalies.
  • Patients receiving anticoagulants e.g. heparin (unfractionated or low molecular weight).
  • Patients with severe IUGR.
  • Patients with accidental hemorrhage.

Trial design

Primary purpose

Diagnostic

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

100 participants in 1 patient group

MgSO4
Experimental group
Description:
The magnesium sulfate will be given according to the regimen of 6 grams intravenous over 20 minutes as a loading dose.
Treatment:
Drug: MgSO4

Trial contacts and locations

1

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Central trial contact

Ahmed Maged, MD; Mohamed Elmahy, MD

Data sourced from clinicaltrials.gov

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