Actively Recruiting
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
Eligibility Criteria
You may qualify if you...
- All hospital records of patients diagnosed as preeclampsia with severe features planned to receive magnesium sulphate.
You will not qualify if you...
- Records with missing data about the regimen of magnesium sulphate used
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
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
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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