Impact of Electronic Cigarettes on Perinatal Immune Responsiveness and Birth Outcomes

Sponsor
Kristin Ashford (Other)
Overall Status
Completed
CT.gov ID
NCT02553577
Collaborator
Virginia Commonwealth University (Other)
278
1
61.5
4.5

Study Details

Study Description

Brief Summary

There has been a dramatic escalation of electronic cigarette (e-cig) use among women of childbearing age, including pregnant women. The overall goal of this study is to determine the effects of e-cigs on prenatal biomarkers and birth outcomes. It is imperative that more data about these effects be available to better inform women of childbearing age.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    The United States has the largest and fastest growing market for electronic cigarettes (e-cigs), and adult women of childbearing age are the most common users. However, no data exist regarding the health effects of e-cigs on pregnant women or their babies. It is well known that tobacco use during pregnancy is the most modifiable risk associated with adverse birth outcome, yet nearly one in four women in Kentucky continue to use tobacco products during pregnancy. E-cigs also contain varied (unregulated) concentrations of nicotine, despite nicotine being classified as a pregnancy class-D drug (exhibiting teratogenic effects on the fetus). The addictive nature of nicotine may explain continued use during this vulnerable time.

    E-cigs have been the center of recent controversy regarding novel smoking cessation or harm reduction products. There is also concern that marketing strategies promoting harm reduction may increase the appeal and obfuscate the known adverse effects of nicotine on fetal development. In addition to the adverse effects of prenatal nicotine, maternal tobacco use alters immune response during pregnancy, placing women at increased risk for preterm birth.

    The overall goal of this study is to determine the effects of e-cigs (and dual use) on perinatal biomarkers and birth outcomes. Three hundred and sixty pregnant women will be recruited. Participants will complete a survey to measure tobacco related behaviors, and provide perinatal biomarkers at four time points (each trimester and postpartum). Data analysis will include a series of repeated ANCOVAs to determine the association of perinatal cigarette smoking (conventional, e-cigarettes-only, and dual use) with perinatal biomarkers. A one-way ANCOVA will be used to determine the association with birth outcomes. Primary biomarker measures include: expired air carbon monoxide, urine and serum cotinine, serum immune markers and urinary NNAL. Gestational age at birth and birth weight are the primary birth outcomes.

    Until more data about the effects of e-cigs and dual use on perinatal immune response and birth outcomes are available, promotion of e-cigs during pregnancy would be premature. There is an urgent need to investigate the impact of e-cigs and dual use on perinatal biomarkers and birth outcomes. The lack of research may unnecessarily place women-and their babies -at risk for lifelong adverse health outcomes.

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    278 participants
    Observational Model:
    Other
    Time Perspective:
    Prospective
    Official Title:
    The Impact of Electronic Cigarettes on Perinatal Immune Responsiveness and Birth Outcomes in Appalachia
    Actual Study Start Date :
    Jan 13, 2016
    Actual Primary Completion Date :
    Feb 28, 2021
    Actual Study Completion Date :
    Feb 28, 2021

    Arms and Interventions

    Arm Intervention/Treatment
    Conventional cigarettes -only

    Women who are pregnant and use conventional tobacco products -only

    Electronic Cigarette (ecig) (ENDS) -ONLY

    Women who are pregnant and use electronic cigarettes (ecigs) -only

    Conventional + ecig use (DUAL)

    Women who are pregnant and use conventional + ecigs (dual)

    Outcome Measures

    Primary Outcome Measures

    1. Gestational age at birth [Up to nine months]

      Investigators will determine if there is a significant difference in gestational age at birth among three groups: pregnant women who use conventional tobacco-only; pregnant women who use e-cig only; and dual users

    Secondary Outcome Measures

    1. Infant birth weight [Up to two hours]

      Investigators will determine if there is a significant difference in birth weight among three groups: pregnant women who use conventional tobacco-only; pregnant women who use e-cig only; and dual users

    2. Change in Prenatal Cytokine level in each trimester and postpartum [14 weeks; 24 weeks; 34 weeks; 48 weeks and up to 64 weeks]

      Investigators will determine if there are significant changes in cytokine level between trimesters based on groups hree groups: pregnant women who use conventional tobacco-only; pregnant women who use e-cig only; and dual users

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 44 Years
    Sexes Eligible for Study:
    Female
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    1. current tobacco use (traditional cigarettes and/or electronic cigarettes ecig, ENDS)

    2. pregnant in the first or second trimester

    3. age 18-44

    4. can read and write in English.

    Exclusion Criteria:

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 University of Kentucky Prenatal Clinics, Good Samaritian and Polk Dalton Lexington Kentucky United States 40356

    Sponsors and Collaborators

    • Kristin Ashford
    • Virginia Commonwealth University

    Investigators

    • Principal Investigator: Kristin B Ashford, PhD, University of Kentucky

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Kristin Ashford, Principal Investigator, University of Kentucky
    ClinicalTrials.gov Identifier:
    NCT02553577
    Other Study ID Numbers:
    • 1R01DA040694-01
    First Posted:
    Sep 17, 2015
    Last Update Posted:
    Jul 7, 2021
    Last Verified:
    Jul 1, 2021
    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
    Keywords provided by Kristin Ashford, Principal Investigator, University of Kentucky
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jul 7, 2021