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Assessing the Usability and Clinical Utility of the Congo Red Dot Test: A Case-control Study

Preeclampsia Clinical Trial

Official title:
Assessing the Usability and Clinical Utility of the Congo Red Dot Test: A Case-control Study

Clinical Trial Summary

A case-control study will evaluate the clinical utility of the Congo Red test GV-005 in following women with a clinical diagnosis of preeclampsia and clinically healthy women in the postpartum period

Clinical Trial Description

A case-control study (n=150) will evaluate the clinical utility of the Congo Red test GV-005 in following women with a clinical diagnosis of preeclampsia and clinically healthy women in the postpartum period. Women with preeclampsia (n=100) (cases) and clinically healthy women (n=50)(controls) who are hospitalized postpartum will be recruited for the trial. All women will be asked to provide a urine sample. Samples will be collected daily during a woman's hospitalization. The Congo Red test GV-005 and a standard urine dipstick proteinuria test will be performed by a lab technician within 72 hours of sample collection. The purpose of this research is to evaluate progression of urine congophilia postpartum by following patients diagnosed with preeclampsia and clinically healthy women. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02610972
Study type Observational
Source Gynuity Health Projects
Contact
Status Completed
Phase
Start date December 1, 2018
Completion date May 30, 2019
View Details
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