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Evaluation of brain network functional imaging in neonatal brain development

Evaluation of brain network functional imaging in neonatal brain development

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2100048619
Enrollment
Unknown
Registered
2021-07-11
Start date
2022-07-01
Completion date
Unknown
Last updated
2022-03-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

preterm, SGA, LGA, perinatal brain injury

Interventions

preterm group:N/A
Developmental group:N/A
brian injury group:N/A

Sponsors

Peking University First Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. The neonates admitted to the neonatal ward of Peking University First Hospital were divided into 4 groups: A preterm group: 32-36 weeks premature infants, a total of 50 cases; B development group: 50 full-term small-for-gestational age infants Cases, 50 large-for-gestational-age infants; C brain injury group: 50 full-term neonates with clear brain injury; D control group: 100 full-term infants suitable for gestational age; 2. Inclusion criteria for ABD neonates: comprehensive clinical manifestations, physical examination, cranial imaging tests, no evidence of brain injury; 3.C Inclusion criteria for neonates: According to the comprehensive diagnosis of clinical symptoms, signs, cranial imaging (ultrasound, MRI), EEG, etc., including: moderate-severe neonatal hypoxic-ischemic encephalopathy, 3- Grade 4 intracranial hemorrhage, perinatal stroke, bilirubin encephalopathy, neonatal bacterial meningitis, metabolic encephalopathy, etc. Taking the common clinical hypoxic-ischemic brain injury as an example, the acute phase occurs within 72 hours after birth, and the clinical manifestations are changes in consciousness, muscle tone, and primitive reflexes, which may be accompanied by convulsions, and the EEG manifests as background activity. Abnormal, brain imaging showed diffuse cerebral edema.

Exclusion criteria

Exclusion criteria: 1. In the process of near-infrared spectral data acquisition, the subjects were crying and difficult to appease, making the acquisition impossible. 2. The tested neonates had head hematoma. 3. Family members refuse to participate in the research.

Design outcomes

Primary

MeasureTime frame
brain network;

Countries

China

Contacts

Public ContactLiu Lili

Beijing University First Hospital

liulili0205@163.com+86 13810536759

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026