Human Epididymis Protein 4 in Women With Severe Preeclampsia / HELLP Syndrome

NCT ID: NCT03891394

Last Updated: 2019-03-28

Study Results

Results pending

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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Recruitment Status

UNKNOWN

Total Enrollment

110 participants

Study Classification

OBSERVATIONAL

Study Start Date

2019-04-01

Study Completion Date

2019-10-30

Brief Summary

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Pre-eclampsia seems to be associated with a four to five times increase risk of later microalbuminuria and CKD which might suggest a possible direct renal damage from pre-eclampsia

Detailed Description

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Conditions

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Preeclampsia

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Interventions

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Human epididymis protein 4

Human epididymis protein 4 serum level in predicting persistent proteniuria

Intervention Type DIAGNOSTIC_TEST

Eligibility Criteria

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Inclusion Criteria

1. Pregnant women 18-35 years old.
2. Fulfilling the criteria for diagnosis of sever preeclampsia.
3. Fulfilling the criteria for diagnosis of HELLP syndrome

Exclusion Criteria

1. Diabetes mellitus
2. Preexisting renal disease.
3. Chronic hypertension
4. Rheumatologic diseases
5. Adnexal mass.
Minimum Eligible Age

18 Years

Maximum Eligible Age

35 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No

Sponsors

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Ain Shams University

OTHER

Sponsor Role lead

Responsible Party

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Radwa Rasheedy Ali

principal investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Other Identifiers

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ainshamHE4

Identifier Type: -

Identifier Source: org_study_id

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