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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02665897
Other study ID # PET
Secondary ID
Status Completed
Phase N/A
First received January 22, 2016
Last updated June 8, 2017
Start date January 2016
Est. completion date May 2017

Study information

Verified date June 2017
Source Assiut University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

In view of both endothelial injury in pre-eclampsia, high blood pressure and kidney impairment characteristics, a recent study demonstrated that the serum levels of NGAL increased at the end of the second trimester in women who subsequently developed pre-eclampsia compared to the control group.

This correlates well with the endothelial damage that occurs during pre-eclampsia and thus NGAL can be considered as a promising marker in predicting both early and late onset pre-eclampsia. It may be required to combine one or more biomarker with NGAL to increase the precision, and sensitivity for detection of risk and reliability of using biomarkers for pre-eclampsia.


Recruitment information / eligibility

Status Completed
Enrollment 90
Est. completion date May 2017
Est. primary completion date December 2016
Accepts healthy volunteers No
Gender Female
Age group 20 Years to 40 Years
Eligibility Inclusion Criteria:

- Age 20-40 years.

- Gestational age >20 weeks.

Exclusion Criteria:

- Patients with preexisting renal disease,hypertension, diabetes mellitus, gestational hypertension.

- Patients Refuse to participate in the study

- Patients already have complicated preeclampsia.

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Egypt Ahmed Abbas Assiut Cairo

Sponsors (1)

Lead Sponsor Collaborator
Assiut University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary The level of circulating NGAL 24 hours