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Lipid Profile as Predictor of Adverse Maternal and Neonatal Outcomes: A Pilot Study

Pregnancy Clinical Trial

Official title:
Lipid Profiles as Predictor of Adverse Maternal and Neonatal Outcomes: A Pilot Study

Clinical Trial Summary

The purpose of this study is to ascertain lipid profiles during pregnancy, specifically during the 24-28 week gestation and again near term at 36 weeks gestation. The research team are investigating whether lipid profiles can predict adverse maternal and neonatal outcomes.

Clinical Trial Description

The purpose of this research is to investigate whether lipids profiles during pregnancy impact LGA and other adverse outcomes in pregnancy. Participants will have blood drawn twice; the first blood work is a fasting blood draw (separate blood draw) on the same day but preceding the standard glucose test. The second blood draw is drawn at the time of routine clinical care (third trimester blood work). Patients will be approached at the time of the anatomy ultrasound for participation. If they consent to participate they will have a FASTING lipid panel drawn at the time of their 24-28w GCT and again at the time of their 36w third trimester labs. Patients will receive a reminder call prior to scheduled 24-28 week appointment for fasting instructions. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05535660
Study type Observational
Source Icahn School of Medicine at Mount Sinai
Contact
Status Active, not recruiting
Phase
Start date July 29, 2022
Completion date October 2024
View Details
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