CompletedNCT03801447

Biomarkers and Preeclampsia Outcomes

Studying Preeclampsia

Last synced from ClinicalTrials.gov

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Key facts

Sponsor
Dacima Consulting
Principal Investigator
Dalenda Chelli, MD
Maternité de la Rabta - Tunis
Enrollment
600 target
Eligibility
20-50 years · FEMALE
Timeline
20182022

Study locations (1)

Collaborators

Maternity Center of Tunis

Primary source

Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.

Open NCT03801447 on ClinicalTrials.gov

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