Skip to main content
OpenTrials
Active, Not Recruiting

NCT Number: NCT04215783

Childhood Allergy and the Neonatal Environment

The purpose of this research study is to study the relationship between childhood asthma, allergies, and early-life environmental factors that may cause childhood asthma and allergies. Previous birth cohort studies have found early-life environmental factors such as allergies, pollutants, viruses and bacteria have all contributed to the development of asthma and allergies. Investigators are doing this research because there continues to be a strong need to understand the root causes of asthma and allergies. The CANOE study is an observational cohort study, which means investigators are not asking participants or participant's child to change their medications and investigators will not be giving participants or participant's child a study drug.

Active, Not Recruiting

This study is active but is not currently recruiting participants.

Key information

Conditions

Asthma in Children Allergy Asthma Bronchial Diseases Hypersensitivity Hypersensitivity, Immediate Immune System Diseases Lung Diseases Lung Diseases, Obstructive Respiratory Hypersensitivity Respiratory Tract Diseases

Sex eligibility

All sexes

Study type

Observational

Primary location

Henry Ford Health Systems, Detroit, Michigan, United States

Loading trial locations.

About this study

The CANOE study will provide an opportunity to collect novel longitudinal samples not available from the current CANOE birth cohorts, as well as enhanced and standardized environmental sampling in early life. One of the main goals of this study is to gather data and specimens, beginning in the prenatal periods, that will assess environmental exposures to toxins and microbes, and host characteristics including genetics, epigenetics, gene expression, the proteome and metabolome, microbial colonization and viral respiratory infections. The main study outcomes will be important interim conditions (e.g., recurrent wheeze, early multiple sensitization) that are highly associated with the development of asthma. Additional outcomes (perinatal outcomes, growth, neurocognitive development) will be collected as part of the collaborative Environmental Influences on Child Health Outcomes (ECHO)-wide Cohort Data Collection Protocol.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • History of or concurrent asthma or allergic rhinitis (hay fever) in either biologic parent or sibling (at least one shared biological parent) by parental report. The presence of paternal or sibling allergy or asthma will be ascertained by maternal report.
  • Maternal age greater than or equal to 18 years at the time of study enrollment.

Exclusion criteria

  • Maternal HIV infection at time of delivery.
  • Plans for the family to move out of the geographic area during the period of the study.
  • Does not speak English.
  • Current maternal use of progesterone during pregnancy to prevent preterm birth.
  • Progesterone use is only an exclusion if currently being taken at time of enrollment for preterm birth. Previous use to prevent preterm birth or use at any time for other indications is allowed.
  • Pregnancy is a result of an embryo donor (egg and sperm donor pregnancies are permitted).
  • Past or current medical problems or findings from physical examination or laboratory testing which, in the opinion of the investigator or designee, may pose additional risks from participation in the study, may interfere with the participant's ability to comply with study requirements or that may impact the quality or interpretation of the data obtained from the study.

Treatment and study plan

Primary outcomes

  1. Number of children with recurrent wheeze

    Time frame: 3 years

    Number of children with recurrent wheezing will be reported. Recurrent wheeze, defined as at least 2 episodes of wheeze with one occurring in the last 12 months of study participation for children between 2 and 3 years of age.

  2. Number of children with early aeroallergen sensitization

    Time frame: 2 years

    Number of children with early aeroallergen sensitization will be reported. Early aeroallergen sensitization, defined as sensitization to at least one aeroallergens by age 2 years.

  3. Number of children diagnosed with asthma

    Time frame: 4 years

    Number of children who diagnosed, either by a doctor or self-report, at age 6 or 7 years.

Secondary outcomes

  1. Number of children with Atopic dermatitis (AD)

    Time frame: 3 years

    Number of children with AD will be reported. Atopic dermatitis, defined if at least 1 of the following is present:

    • Physician diagnosis of eczema/AD (either study physician or other physician by parental report) at any time,
    • Objective SCORAD (SCORing Atopic Dermatitis) ≥ 8 at 1 or more study assessments. The range of the objective SCORAD lies between 0 and 83. Based on the objective SCORAD, the severity of AD can be classified into mild (<15), moderate (between 15 and 40) and severe (greater than or equal to 40) AD.
    • Parent report of an itchy rash outside of the diaper area lasting for at least 7 days and not diagnosed as another condition.

  2. Number of children with food allergies

    Time frame: 3 years

    Number of children with the food allergy will be reported. Food allergy defined as typical signs and symptoms of immediate IgE (Immunoglobulin E) -mediated reaction (such as urticaria, angioedema, vomiting, wheezing, cough, hypotension) within 2 hours of food ingestion and with positive immunocap testing to that food.

  3. Lung function

    Time frame: 4 years

    Lung function is assessed by spirometry, a 10-15 minute, non-invasive, and painless test that requires participants to breathe through a mouthpiece connected to a computer, often with a nose clip to prevent air leaks. Spirometry measures lung function by calculating the volume and speed of air exhaled, and is reported as a ratio of the two.

Sponsors and collaborators

Lead sponsor

University of Wisconsin, Madison

Other

Collaborators

  • Duke University
  • National Institute of Allergy and Infectious Diseases (NIAID)
  • National Institutes of Health (NIH)

Registry information

Acronym: CANOE

Important dates

Study start
2020
Primary completion
2027
Study completion
2027
First posted
Jan 2, 2020
Registry last updated
Feb 10, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Related clinical trials

Published trials that share one or more normalized conditions with this study.