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MRI for Early Cerebral Palsy Prediction in Infants with White Matter Injury

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What is being collected

Data Collection

Collected from today forward - Prospective
Who is being recruted

Brain Damage, Chronic+2

+ Brain Diseases

+ Central Nervous System Diseases

From 6 Months to 2 Years
+5 Eligibility Criteria
See all eligibility criteria
How is the trial designed

Cohort

Tracking disease incidence in order to identify risk factors and understand disease progression over time.
Observational
Study Start: September 2024
See protocol details

Summary

Principal SponsorFirst Affiliated Hospital Xi'an Jiaotong University
Study ContactYitong Bian, MD
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Study start date: September 1, 2024

Actual date on which the first participant was enrolled.

Cerebral palsy (CP) is a common group of movement disorders that often results in disability in children. In the context of CP, the importance of early diagnosis is crucial, but current diagnostic modalities often identify cases after the age of 2 years. After initial screening of infants at high risk for CP by behavioral scoring, magnetic resonance imaging (MRI) forms an integral part of the comprehensive evaluation. The training of conventional model of CP risk prediction requires a large investment of time and financial resources. The average sensitivity rate drops to 90%. Up to now, deep learning technology has been widely used in tasks related to image-based disease classification and has shown excellent performance. Periventricular white matter injury (PVWMI) accounts for the largest proportion of various types of brain injuries in cerebral palsy, and the types of brain injuries in cerebral palsy are rich and complex, posing difficulties and challenges to deep learning models. Therefore, this study focuses on PVWMI, the most common type of cerebral palsy, and uses conventional MRI to develop a deep learning prediction model for CP in infants aged 6 months to 2 years old.

Official TitleEarly Prediction of Cerebral Palsy by MRI in Infants With White Matter Injury: a Multicenter Study
NCT06575283
Principal SponsorFirst Affiliated Hospital Xi'an Jiaotong University
Study ContactYitong Bian, MD
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

1000 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Cohort

These studies follow a group of individuals with common characteristics (such as a condition or birth year) over a specific period to study health outcomes or exposures.

Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

From 6 Months to 2 Years

Range of ages for which participants are eligible to join.

Healthy volunteers allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

Brain Damage, ChronicBrain DiseasesCentral Nervous System DiseasesCerebral PalsyNervous System Diseases

Criteria

3 inclusion criteria required to participate
Infants and children at high risk of periventricular white matter injury (PVWMI) (gestational age <35 weeks, birth weight <2.6 kg, forceps-assisted delivery/fetal head attraction, Apgar score <7, hypoglycaemia, sepsis, electrolyte disturbances, premature rupture of membranes);

Those who underwent MRI at 6 months of age-2 years, including at least T1WI and T2WI sequences;

Upon follow-up, the patient's clinical diagnosis: cerebral palsy, other diagnoses that did not develop into cerebral palsy, or inability to confirm the diagnosis).

2 exclusion criteria prevent from participating
Incomplete MRI images or unreadable images due to motion artefacts;

Incomplete neurobehavioural assessment data (including: gross motor function).

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Study Objectives

Study Objectives

Primary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 1 location

Suspended

The First Affiliated Hospital of Xi'an Jiaotong University

Xi'an, ChinaOpen The First Affiliated Hospital of Xi'an Jiaotong University in Google Maps
Recruiting soonOne Study Center