Pregnancy and Early Neurodevelopmental Outcomes Following In Utero Lyme Disease Exposure

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorChildren's National Research Institute

About this trial

The purpose of this pilot study is to assess the feasibility of longitudinal neurodevelopmental evaluation of fetuses and infants exposed to Lyme disease in utero. Participants with Lyme disease or Post-Treatment Lyme Disease Syndrome (PTLDS) will be recruited during pregnancy. Pregnancies will be monitored and infant development will be assessed from birth until age 18 months.

Eligibility criteria

Qualifiers

English speaker

Currently reside in the United States or Canada

Meet CDC criteria for: (1) clinical and/or laboratory diagnosis of Lyme disease during any stage of current pregnancy, OR (2) clinical diagnosis of PTLDS/Chronic Lyme within 3 years of current pregnancy

Able to be contacted for follow-up

Disqualifiers

Intellectually unable to comprehend study procedures

Health issues or metallic implant that precludes undergoing MRI

Incapable of completing study requirements (note: inability to travel to Children's National for in-person follow-up [for example, due to bedrest, travel restrictions, or financial inability to travel] is NOT an exclusion criterion; any interested and eligible participants requiring "remote only" participation will be permitted to join the study and complete all requirements besides in-person follow-up)

Trial design

Treatments tested in this trial

  • Neurodevelopmental assessments and follow-up

Treatment groups

40 Participants
are divided into 2 treatment groups

Sponsors and collaborators

Children's National Research Institute

Lead sponsor

Clinical Trials Network for Lyme and Other Tick-Borne Diseases

Collaborator

Steven & Alexandra Cohen Foundation

Collaborator