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
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