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Analysis of Biological Progression and Regression of HELLP Syndrome in Time

Recruiting
Conditions
HELLP Syndrome
Preeclampsia
Registration Number
NCT06758960
Lead Sponsor
CHU Mohammed VI Marrakech
Brief Summary

Prospective observational study about progression and regression of biological parameters of HELLP syndrome

Detailed Description

Data collection included a comprehensive review of pathological histories, identification of complications based on clinical presentation, daily monitoring of biological parameters, documentation of transfusion events, recording of corticosteroid administration according to gestational age, and detailed reporting of extraction and analgesia techniques.

Recruitment & Eligibility

Status
RECRUITING
Sex
Female
Target Recruitment
70
Inclusion Criteria
  • Pregnant women who are admitted to the maternal ICU for a biological HELLP syndrome
Exclusion Criteria
  • Patients whose biological presentation was attributable to other conditions, such as microangiopathies or leukemia.
  • Patients who benefited from plasma exchange therapy

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Platelets countUp to 10 days

Platelets count will be monitored daily before and after delivery

Secondary Outcome Measures
NameTimeMethod
Concentration of Lactate dehydrogenaseUp to 10 days

Monitored daily before and after delivery

Concentration of Liver enzymesUp to 10 days

daily monitoring of alkaline phosphatase, alanine transaminase before and after delivery

Trial Locations

Locations (1)

CHU Mohammed VI of Marrakech

🇲🇦

Marrakech, Marrakech - Safi, Morocco

CHU Mohammed VI of Marrakech
🇲🇦Marrakech, Marrakech - Safi, Morocco
Nizar Amllah, M.D
Contact
+212 613069684
nizaramllah@gmail.com

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