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NCT05283473Completed

Serum Magnesium Concentration in Magnesium Sulfate Therapy for Severe Preeclampsia

Serum Concentration of Magnesium Attained in Magnesium Sulfate Therapy in Pregnant Women With Severe Preeclampsia

Source: ClinicalTrials.gov · Last updated 7 Jan 2025

Brief summary (registry, in English)

Pregnant women diagnosed with pre-eclampsia with severe features will be treated with magnesium sulfate to prevent seizures. Magnesium sulfate will be administered according to My Duc Hospital's protocol for treatment of pre-eclampsia (a loading dose of 4.5g given intravenously in 20 min, followed by a maintenance dose at an infusion rate of 1.5g/h). Serum magnesium concentrations will be measured before the loading dose and 0.5h, 1h, 2h, and every 6 hours thereafter.

Status (registry)
Completed
Study type
Observational
Enrollment
64 (actual)
First submitted
12 Feb 2022
Start date
15 Mar 2022
Primary completion date
21 Feb 2024
Lead sponsor
Mỹ Đức Hospital
NCT number
NCT05283473

What you commit to

  • Study type: Observational
  • Participants enrolled: 64
  • From 15 Mar 2022 to the primary completion date, 21 Feb 2024
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Known hypersensitivity to the drug,

Lab values

  • Impaired renal function (eGFR \< 60 mL/min/ 1,73 m2 or oliguria )
  • Occurrence of eclampsia before magnesium sulfate administration

Other

  • Severe myasthenia, atrioventricular block
  • A diminished level of consciousness.

Who the study is looking for

  • Pregnant women
  • Aged ≥ 18
  • Diagnosed with pre-eclampsia with severe features, with or without chronic hypertension, as defined by the American College of Obstetricians and Gynecologists (ACOG) diagnosis criteria.
  • Provision of written informed consent to participate as shown by a signature on the patient consent form.

Age in the registry: 18 years to - · Sex: Female · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
My Duc Hospital
Coordinator of this site? Confirm its status
Ho Chi Minh CityVietnamUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.