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

Sponsor
Icahn School of Medicine at Mount Sinai (Other)
Overall Status
Recruiting
CT.gov ID
NCT05535660
Collaborator
(none)
50
1
11
4.5

Study Details

Study Description

Brief 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.

Condition or Disease Intervention/Treatment Phase

    Detailed 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

    Study Type:
    Observational
    Anticipated Enrollment :
    50 participants
    Observational Model:
    Cohort
    Time Perspective:
    Prospective
    Official Title:
    Lipid Profiles as Predictor of Adverse Maternal and Neonatal Outcomes: A Pilot Study
    Actual Study Start Date :
    Jul 29, 2022
    Anticipated Primary Completion Date :
    Jun 30, 2023
    Anticipated Study Completion Date :
    Jun 30, 2023

    Arms and Interventions

    Arm Intervention/Treatment
    LGA neonates

    Researchers will compare lipid levels in large for gestational age (LGA) and non-LGA neonates.

    non-LGA neonates

    Researchers will compare lipid levels in large for gestational age (LGA) and non-LGA neonates.

    Outcome Measures

    Primary Outcome Measures

    1. Neonatal birthweight [at birth, day 1]

      Neonatal birthweight will be classified as large for gestational age (LGA) or non-LGA

    Secondary Outcome Measures

    1. Number of participants with preeclampsia [at birth, day 1]

    2. Number of participants with gestational diabetes [at birth, day 1]

    3. Total Cholesterol [at 24-28 weeks gestation]

      Total Cholesterol obtained while fasting at 24-28 weeks gestation. Different blood tests can be done to measure each type of cholesterol. Total cholesterol level measures all types of cholesterol in the blood.

    4. Total Cholesterol [at 36 weeks gestation]

      Total Cholesterol obtained while fasting at 36 weeks gestation. Different blood tests can be done to measure each type of cholesterol. Total cholesterol level measures all types of cholesterol in the blood.

    5. High-Density Lipoprotein Cholesterol (HDL) [at 24-28 weeks gestation]

      High-Density Lipoprotein Cholesterol (HDL) obtained while fasting at 24-28 weeks. HDL helps keep arteries open and reduces the risk for heart attack. High levels of HDL may be nearly as protective for the heart as low levels of LDL

    6. High-Density Lipoprotein Cholesterol (HDL) [at 36 weeks gestation]

      High-Density Lipoprotein Cholesterol (HDL) obtained while fasting at 36 weeks. HDL helps keep arteries open and reduces the risk for heart attack. High levels of HDL may be nearly as protective for the heart as low levels of LDL

    7. Triglycerides [at 24-28 weeks gestation]

      Triglycerides obtained while fasting at 24-28 weeks gestation. Triglycerides interact with HDL cholesterol in such a way that HDL levels fall as triglyceride levels rise. High triglyceride levels are also associated with the inflammatory response -- the harmful effect of an overactive immune system that can cause considerable damage to cells and tissues, including the arteries.

    8. Triglycerides [at 36 weeks gestation]

      Triglycerides obtained while fasting at 36 weeks gestation. Triglycerides interact with HDL cholesterol in such a way that HDL levels fall as triglyceride levels rise. High triglyceride levels are also associated with the inflammatory response -- the harmful effect of an overactive immune system that can cause considerable damage to cells and tissues, including the arteries.

    9. Low-Density Lipoprotein Cholesterol (LDL) [at 24-26 weeks gestation]

      Low-Density Lipoprotein Cholesterol (LDL) obtained while fasting at 24-28 weeks gestation. Low-density lipoprotein (LDL) transports about 75% of the blood's cholesterol to the body's cells. Heart disease is least likely to occur among people with the lowest LDL levels. Lowering LDL is the primary goal of cholesterol drug and lifestyle therapy.

    10. Low-Density Lipoprotein Cholesterol (LDL) [at 36 weeks gestation]

      Low-Density Lipoprotein Cholesterol (LDL) obtained while fasting at 36 weeks gestation. Low-density lipoprotein (LDL) transports about 75% of the blood's cholesterol to the body's cells. Heart disease is least likely to occur among people with the lowest LDL levels. Lowering LDL is the primary goal of cholesterol drug and lifestyle therapy.

    11. Very-low-density Lipoprotein Cholesterol (VLDL) [at 24-26 weeks gestation]

      Very-low-density Lipoprotein Cholesterol (VLDL) obtained while fasting at 24-28 weeks gestation. VLDL is one of the three main types of lipoproteins. Lipoproteins are made up of cholesterol, triglycerides, and proteins. They move cholesterol, triglycerides, and other lipids (fats) around the body.

    12. Very-low-density Lipoprotein Cholesterol (VLDL) [at 36 weeks gestation]

      Very-low-density Lipoprotein Cholesterol (VLDL) obtained while fasting at 36 weeks gestation. VLDL is one of the three main types of lipoproteins. Lipoproteins are made up of cholesterol, triglycerides, and proteins. They move cholesterol, triglycerides, and other lipids (fats) around the body.

    13. Total Cholesterol/HDL Ratio [at 24-26 weeks gestation]

      Total Cholesterol/HDL Ratio obtained while fasting at 24-28 weeks gestation. The total cholesterol /HDL ratio is the proportion of one type of cholesterol to all the other cholesterol in the blood. Total cholesterol includes three substances HDL, LDL, and VLDL. Higher ratios indicate greater risk of heart coronary heart disease.

    14. Total Cholesterol/HDL Ratio [at 36 weeks gestation]

      Total Cholesterol/HDL Ratio obtained while fasting at 36 weeks gestation. The total cholesterol /HDL ratio is the proportion of one type of cholesterol to all the other cholesterol in the blood. Total cholesterol includes three substances HDL, LDL, and VLDL. Higher ratios indicate greater risk of heart coronary heart disease.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 45 Years
    Sexes Eligible for Study:
    Female
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • Singleton pregnancy

    • Ages 18-45

    • Presentation to prenatal care by the 2nd trimester

    • Prenatal care at Mount Sinai Hospital

    • Anticipated delivery at Mount Sinai Hospital

    Exclusion Criteria:
    • Multiple gestations

    • Preexisting hyperlipidemia

    • Preexisting diabetes

    • Delayed presentation to prenatal care after the 2nd trimester 5. Prenatal care or delivery outside of Mount Sinai Health System

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Mount Sinai OBGYN Faculty Practice Associates New York New York United States 10029

    Sponsors and Collaborators

    • Icahn School of Medicine at Mount Sinai

    Investigators

    • Principal Investigator: Luciana Vieira, MD, MS, Icahn School of Medicine at Mount Sinai

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Luciana Vieira, Assistant Professor, Icahn School of Medicine at Mount Sinai
    ClinicalTrials.gov Identifier:
    NCT05535660
    Other Study ID Numbers:
    • STUDY-21-01936-MOD002
    First Posted:
    Sep 10, 2022
    Last Update Posted:
    Sep 10, 2022
    Last Verified:
    Sep 1, 2022
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Product Manufactured in and Exported from the U.S.:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Sep 10, 2022