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Clinical Trial Summary

This study aims to compare between androgens level (serum total and free testosterone) in women with preeclampsia and normal ones in the third trimester of pregnancy (28-40 weeks).


Clinical Trial Description

Methodology:

All women in this study will be subjected to:

- All women are candidates for this study according to inclusion and exclusion criteria.

- History taking with special emphases on last menstrual period to determine the exact Gestational age.

- A reliable date is defined as the occurrence of regular menstrual cycles (28±7 days) in patients who have not taken oral contraceptives during the three months before conception and have no irregular bleeding.

- General and abdominal examination for each patient to determine those patients matching with the inclusion criteria.

- Preeclampsia refers to the new onset of hypertension (systolic blood pressure ≥140 mmHg ,or diastolic blood pressure≥ 90 mmHg ,or both, measured on two occasions > 6 hours apart) and either proteinuria or end organ dysfunction after 20 weeks of gestation in a previously normotensive woman.

- At Ain Shams University Hospitals, the investigator will use ELISA based test system intended for the quantitative measurement of total and free testosterone for patients of both groups. ;


Study Design

Observational Model: Case Control, Time Perspective: Retrospective


Related Conditions & MeSH terms


NCT number NCT02992145
Study type Observational
Source Ain Shams Maternity Hospital
Contact
Status Completed
Phase N/A
Start date March 2016
Completion date December 2016

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