Association Between Pococyturia and Pre-eclampsia Severity
NCT ID: NCT03316391
Last Updated: 2025-07-24
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
14 participants
OBSERVATIONAL
2019-05-22
2021-03-02
Brief Summary
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Detailed Description
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Conditions
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Study Design
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CASE_ONLY
PROSPECTIVE
Study Groups
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Pre-eclampsia
Patients in hospital for pre-eclampsia at the Hopital Femme-Mère-Enfant
Dosage of urinary podocyturia
Dosage of urinary podocyturia at admission, delivery and post-partum visit
Interventions
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Dosage of urinary podocyturia
Dosage of urinary podocyturia at admission, delivery and post-partum visit
Eligibility Criteria
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Inclusion Criteria
* single pregnancy
* admission for pre-eclampsia
* patient receiving information and non-opposition to participate
Exclusion Criteria
* in utero fetal demise excepted if associated with pre-eclampsia
* antecedent of nephropathy
* fetal malformation, chromosomal anomalies
* inability to understand information provided
* prisoner or under administrative supervision
18 Years
FEMALE
No
Sponsors
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Hospices Civils de Lyon
OTHER
Responsible Party
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Locations
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Service de gynécologie-obstétrique
Pierre-Bénite, Rhône, France
Department of obstetrics, Femme Mère Enfant Hospital, Lyon, France
Bron, , France
Countries
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Other Identifiers
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69HCL17_0517
Identifier Type: -
Identifier Source: org_study_id
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