Home › Brain Hypoxia-Ischemia › NCT07165938

Genetics of Neonatal Encephalopathy and Related Disorders

Who can join

All ages · All sexes

Proband Criteria:

Inclusion Criteria:

* Diagnosed with neonatal encephalopathy during the neonatal period as documented in the electronic medical record
* Less than 6 years old at the time of study enrollment
* Patient at Boston Children's Hospital

Exclusion Criteria:

* Genetic cause of NE already identified
* Deceased prior to enrollment

Parent criteria:

Inclusion Criteria:

\- Biological parent of eligible proband (see above)

About the study

Investigators at Boston Children's Hospital are conducting research in order to better understand the genetic factors which may contribute to neonatal encephalopathy (NE) and related disorders. These findings may help explain the broad spectrum of clinical features and outcomes seen in individuals with a history of NE.

Sponsor: Boston Children's Hospital · Participants: 300 · Started: Feb 4, 2026

Contact the study team

Official record on ClinicalTrials.gov — NCT07165938

Locations in the U.S.

Conditions

• Brain Hypoxia-Ischemia

From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.