Actively Recruiting
Incidence of Postoperative Diaphragmatic Dysfunction in Pregnant Women With Preeclampsia
Led by Cairo University · Updated on 2026-03-11
52
Participants Needed
1
Research Sites
42 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Preeclampsia with severe features remains a leading contributor to maternal morbidity and mortality, particularly in low- and middle-income countries. It is defined by hypertension and involvement of multiple organ systems, including renal, hepatic, hematologic, and neurologic pathways. The interplay of endothelial dysfunction, capillary leakage, and disrupted fluid balance in these patients increases their susceptibility to perioperative pulmonary complications. Although respiratory complications in preeclampsia are clinically significant, the true incidence of postoperative diaphragmatic dysfunction in women with severe disease is not well established. Existing literature largely emphasizes general respiratory failure, pulmonary edema, or the need for mechanical ventilation, rather than specifically evaluating diaphragmatic performance with objective methods such as ultrasound. The current study sought to determine the incidence and identify risk factors for postoperative diaphragmatic dysfunction in women with severe preeclampsia following cesarean delivery.
CONDITIONS
Official Title
Incidence of Postoperative Diaphragmatic Dysfunction in Pregnant Women With Preeclampsia
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients with severe preeclampsia undergoing cesarean section
- Gestational age > 32 weeks
- Female patients aged between 20 and 40 years
You will not qualify if you...
- Age less than 20 years
- Diabetes
- Neuromuscular diseases
- Patient refusal to participate
- Contraindications to magnesium sulphate administration
- Inability to obtain adequate ultrasound views
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
Cairo University Hospitals
Cairo, Egypt
Actively Recruiting
Research Team
M
Mina Adolf Helmy, MD
CONTACT
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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