Actively Recruiting

Age: 18Years +
FEMALE
ID06791668

Comparison of Different Regimens of Magnesium Sulphate in Patients With Severe Preeclampsia at Ain Shams University Maternity Hospital (Retrospective Study)

Led by Ain Shams Maternity Hospital · Updated on 2025-01-24

400

Participants Needed

1

Research Sites

12 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This research aims to learn about the effects of different magnesium sulphate treatment plans for pregnant women with severe pre-eclampsia, a condition that raises blood pressure and may cause seizures. The study focuses on understanding the various ways magnesium sulphate is used to prevent seizures in these women. It is a retrospective observational study reviewing data from the past five years at Ain Shams University Maternity Hospital. The study involves reviewing hospital records to describe magnesium sulphate regimens given to women diagnosed with severe pre-eclampsia. Researchers will examine details like dosage, administration routes, timing before and after delivery, and any changes in treatment. They will also note any side effects, signs of magnesium toxicity, seizure occurrences despite treatment, and related complications such as ICU admissions or postpartum issues. Participants' past medical data will be collected and analyzed, including lab results, vital signs, and delivery details. The study measures outcomes like seizures within 24 hours of delivery, ICU admissions, magnesium toxicity, and postpartum hemorrhage. Confidentiality will be maintained, and the research will provide insights into how different magnesium sulphate regimens affect women with severe pre-eclampsia.

CONDITIONS

Brief Title

Different Regimens of Magnesium Sulphate in Patients With Severe Preeclampsia

Who Can Participate

Age: 18Years +
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • All hospital records of patients diagnosed as preeclampsia with severe features planned to receive magnesium sulphate.
Not Eligible

You will not qualify if you...

  • Records with missing data about the regimen of magnesium sulphate used

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Monitoring

Duration - Review of hospital records from the past 5 years

Participants who have undergone routine care for severe preeclampsia are observed retrospectively to describe different magnesium sulphate regimens and associated outcomes such as eclamptic fits, side effects, and complications.

No visits required; data collected from existing records

Trial Site Locations

Total: 1 location

1

Ain Shams University Maternity Hospital

Cairo, Egypt

Actively Recruiting

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Research Team

R

Rania HM Ahmed, MD

S

Sherif Ashoush, MD

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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