The Heartland Study

Part of paid clinical trials in Indianapolis, Indiana.

Sponsor
Heartland Health Research Alliance
Study ID
NCT05492708
Status
Recruiting

Conditions

  • Birth Defect
  • Exposure to Herbicides
  • Gestational Age and Weight Conditions
  • Miscarriage
  • Pregnancy Complications
  • Pregnancy Related
  • Spontaneous Abortion

Eligibility Criteria

Sex
FEMALE
Age
18 Years - N/A
Healthy Volunteers
Accepted

Study Details

The Heartland Study is a prospective, observational study that will enroll up to 2,600 pregnant participants across the Heartland States in the U.S.. The objective of the Heartland Study is to address major knowledge gaps concerning the health effects of herbicides on maternal and infant health. The study is being conducted to evaluate the associations between environmental exposures to herbicides during and after pregnancy and reproductive health outcomes. The study is measuring multiple biomarkers of herbicide exposure among pregnant Midwesterners and their partners to evaluate associations with pregnancy and childbirth outcomes, epigenetic biomarkers of exposure, and child development.

Key Dates

Start date
Jan 11, 2020
Status verified
Jun 2025
Primary completion
Jan 31, 2027
Completion
Jan 31, 2029

Study Design

Enrollment
2,600 participants (estimated)

Primary Outcome Measure

Pregnancy loss [ Time Frame: Enrollment to birth ]

Central Contacts

Locations (4)

FacilityCityStateZIPSite coordinators
Indiana University Medical CenterIndianapolisIndiana46202
Kathleen Flannery
David Haas, MD (PRINCIPAL_INVESTIGATOR)
University of Iowa Health CareIowa CityIowa52242
Donna Santillan, PhD
Ashlyn Kenney
Gundersen HealthLa CrosseWisconsin54601-
Marshfield ClinicMarshfieldWisconsin54449
Melissa Slager
Peter Johnson, MD (PRINCIPAL_INVESTIGATOR)

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