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Healthy Little Eyes

University of Wisconsin, Madison · with Meriter Foundation · NCT05971446

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Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.

Key facts

Compensation
Not posted. Ask the study team before screening.
Who can join
Up to age 3 · All sexes
Healthy volunteers
Accepted
Study type
Observational
Target enrollment
125
US sites recruiting
1
Study start
February 24, 2020
Record last updated
May 14, 2026

Status re-checked against ClinicalTrials.gov within the last 12 hours.

What the study is about

The purpose of this research study is to gather more information on how eye injury is related to a baby's future development and see if eye function and brain test results can be used, along with current measures, to better diagnose and treat babies with hypoxic-ischemic encephalopathy (HIE).

Participants will undergo up to two eye exam sessions, involving both Visual Evoked Potential (VEP) and Electroretinogram (ERG) exams.

Being studied: Visual Evoked Potential (VEP); Electroretinogram (ERG)

Conditions: Hypoxic-Ischemic Encephalopathy; Neonatal Encephalopathy; Encephalopathy

Eligibility criteria

Copied from the official record. The study team makes the final decision at screening.

Show full criteria

HIE Neonate Inclusion Criteria

  • Inpatient Neonates diagnosed with HIE
  • Pediatric patients who are less than 78 hours of age at the time of enrollment
  • Participants whose parent/legal guardian is able to complete consenting process in English

HIE Neonate Exclusion Criteria

  • Participants with prenatally diagnosed or congenital brain and/or eye abnormalities not associated with HIE, including but not limited to microphthalmia, anophthalmia, congenital cataract, eye or eyelid coloboma, congenital glaucoma, CMV retinitis, optic nerve hypoplasia, aniridia, cryptophthalmos, globe abnormalities
  • Participants who have a known central nervous system illness other than HIE, including but not limited to congenital brain malformations or congenital hydrocephalus
  • Participants whose parent/legal guardian is unable to provide informed consent, including participants who are in foster care, participants within state custody, and participants of minor parents

Waisman, AFCH NBFU, or CERU Clinic HIE Patient Inclusion Criteria:

  • Pediatric patients who have a diagnosis of HIE and present to the Newborn Follow Up Clinic
  • Pediatric patients who are less than 36 months of age at the time of enrollment
  • Participants whose parent/legal guardian is able to complete consenting process in English

Waisman, AFCH NBFU, or CERU Clinic HIE Patient Exclusion Criteria:

  • Participants with prenatally diagnosed or congenital brain and/or eye abnormalities not associated with HIE, including but not limited to microphthalmia, anophthalmia, congenital cataract, eye or eyelid coloboma, congenital glaucoma, CMV retinitis, optic nerve hypoplasia, aniridia, cryptophthalmos, globe abnormalities
  • Participants who have a known central nervous system illness not associated with HIE and its complications. Complications may include seizures, hydrocephalus, and stroke, which are NOT exclusionary. Examples of exclusionary conditions include but are not limited to traumatic brain injury outside the perinatal period, meningitis, or diagnosis of brain tumor
  • Participants whose parent/legal guardian is unable to provide informed consent, including participants who are in foster care, participants within state custody, and participants of minor parents

Well Baby Inclusion Criteria

  • Patient in Meriter's Newborn Nursery
  • ≥37 and \<42 weeks gestational age
  • 5-minute Apgar Score ≥7
  • Occipital Frontal Circumference (OFC) is within average limits for age (\<97th percentile and >3rd percentile)

Well Baby Exclusion Criteria

  • Admitted to the NICU for any reason
  • Known genetic abnormality
  • Diagnosed with HIE
  • Diagnosed with Hypoglycemia
  • Diagnosed with Hyperbilirubinemia requiring phototherapy
  • Identified prenatal exposure to substances, including illicit drugs, alcohol, and/or tobacco
  • Known or suspected neonatal infection requiring treatment (e.g., antibiotics)
  • TORCH infections
  • Abnormal newborn hearing screen
  • Abnormal toxicology screening
  • Identified as large for gestational age (LGA) or small for gestational age (SGA)
  • Participants with prenatally diagnosed or congenital eye abnormalities, including but not limited to microphthalmia, anophthalmia, congenital cataract, eye or eyelid coloboma, congenital glaucoma, CMV retinitis, optic nerve hypoplasia, aniridia, cryptophthalmos, globe abnormalities, and nystagmus
  • Subjects who have a known central nervous system illness or malformation, including but not limited to congenital brain malformations or congenital hydrocephalus
  • Participants whose parent/legal guardian is unable to provide informed consent, including subjects who are in foster care, subjects within state custody, and subjects of minor parents
  • The attending medical team does not approve

Recruiting US locations

  • University of Wisconsin

    Madison, WI 53705

    Site contact: Alexandra Lindstrom · aklinidstrom2@wisc.edu

Study contacts (from the official record)

  • Alexandra Lindstrom · 608-262-2388 · aklindstrom2@wisc.edu
Healthy Little Eyes (NCT05971446) | Bored Studies