Periventricular Leukomalacia

3

Review clinical trials related to Periventricular Leukomalacia. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Neonatal White Matter Injury Trial (WRAP)

The researchers are investigating a new treatment for white matter injury, which is a common type of brain injury in premature babies. The drug, clemastine, is experimental. This means that the drug is not approved by the Food and Drug Administration (FDA) for the treatment of white matter injury. The main purpose of this study is to learn whether clemastine is safe to give to infants with white matter injury. The researchers also want to understand how much clemastine gets into an infant's body when the medication is taken by mouth, and how long it stays in the body.

Participants needed: 24
Trial details
Phase: Phase 1Age: 3-20Biological sex: AllType: InterventionalSponsor: Bridget LaMonica Ostrem, M.D., Ph.D.Updated: Jul 28, 2026Locations: 1
Eligibility criteria

Born at ≤32 weeks gestational age based on prenatal ultrasound or last menstrual... [+4]

Known or suspected metabolic or chromosomal disorder or major congenital anomali... [+12]

Status: Recruiting

Spinal Stimulation and Mobility Devices

This research study will combine non-invasive spinal stimulation with mobility devices to examine the acute impact of the individual and combined effects of these innovative techniques on mobility in children with cerebral palsy.

Participants needed: 20
Trial details
Age: 4-70Biological sex: AllType: InterventionalSponsor: University of WashingtonUpdated: Aug 13, 2025Locations: 1
Eligibility criteria

have a neurologic condition [+5]

have significant medical disease; including uncontrolled systemic hypertension w... [+9]

Status: Not yet recruiting

PUFAs in Preterm Infants

The research endeavors to examine the critical composition of Polyunsaturated Fatty Acids (PUFAs) in premature infants across different gestational stages and under varying disease conditions, and delineate the metabolic attributes of PUFAs in premature infants and their interplay with the onset of diseases. This study anticipates furnishing a theoretical foundation for the rationalization of PUFAs supplementation in premature infants and for informing strategies related to disease prevention and management.

Participants needed: 600
Trial details
Biological sex: AllType: ObservationalSponsor: The First Hospital of Jilin UniversityUpdated: Sep 21, 2023
Eligibility criteria

Not listed