- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05322980
Summary of Infants Weighing 500 Grams or Less
Microcephaly At Birth As a Potential Predictor of Poor Prognosis in Infants Weighing 500 Grams or Less: a Retrospective Cohort Study
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
This is a retrospective single-center cohort study. The study setting is a level IV neonatal intensive care unit (NICU) at Nagano Children's Hospital in Nagano, Japan. We will retrospectively collect the data of those who were admitted to Nagano Children's Hospital NICU between January 1, 2015, and December 31, 2019. Eligible infants will be identified using our neonatal database and clinical records. The extracted data includes maternal background information and clinical course, infant's status at birth, the clinical course in NICU, and the follow-up data at 6 and 18 months of corrected age.
Among the eligible infants, those with a z score of birth head circumference < -2 will be classified into the Microcephaly group and others into the Control group. The z score is calculated using the Japanese growth standard.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
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Nagano
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Azumino, Nagano, Japan, 399-8288
- Nagano Children's Hospital
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Live-born infants weighing ≤ 500 g at birth
- Infants whose clinical course is available in the electronic medical record
Exclusion Criteria:
- Stillbirths
- Infants who received only palliative care at birth
- Outborn infants
- Infants whose assessment at 3 years of age not completed at data analysis
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
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Microcephaly
Infants with primary microcephaly.
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Those with a z score of birth head circumference < -2 (primary microcephaly) are classified into the Microcephaly group.
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Control
Infants without primary microcephaly.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Rate of neurodevelopmental impairment
Time Frame: 3 years of age
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Having at least one of the following conditions: cognitive impairment, cerebral palsy, visual impairment, or hearing impairment.
Cognitive impairment was defined as a modified DQ score of ≤ 70 using the Kyoto Scale of Psychological Development.
CP was defined as (1) a non-progressive disorder of the central nervous system appearing in the early years of life and clinically characterized by a persistent but not unchanging impairment of movement and posture and/or (2) the Gross Motor Function Classification System level ≥ II.
Visual impairment was defined as unilateral or bilateral blindness, or any other condition requiring corrective lenses, which were diagnosed or determined by ophthalmologists.
Hearing impairment was defined as unilateral or bilateral hearing loss that requires a hearing aid.
The diagnosis of hearing loss was made by otolaryngologists using auditory steady-state response.
|
3 years of age
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Survival rate
Time Frame: At discharge from neonatal intensive care unit, an average at 40 weeks' postmenstrual age.
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Survival rate is the proportion of those have survived.
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At discharge from neonatal intensive care unit, an average at 40 weeks' postmenstrual age.
|
|
Rate of severe bronchopulmonary dysplasia
Time Frame: At 36 weeks' postmenstrual age
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The definition of bronchopulmonary dysplasia proposed by the National Institute of Child Health and Human Development is used to classify the severity of bronchopulmonary dysplasia.
Those who need ≥ 30% of oxygen or any mechanical respiratory support at 36 weeks of gestation are classified as having severe bronchopulmonary dysplasia.
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At 36 weeks' postmenstrual age
|
|
Rate of need for surgery for patent ductus arteriosus
Time Frame: In neonatal intensive care unit, an average of up to 4 weeks of life
|
Patent ductus arteriosus is diagnosed by neonatologists using echocardiography and clinical signs.
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In neonatal intensive care unit, an average of up to 4 weeks of life
|
|
Rate of severe intraventricular hemorrhage
Time Frame: In neonatal intensive care unit, an average of up to 2 weeks of life
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Intraventricular hemorrhage is diagnosed by neonatologists using head ultrasound.
Severe IVH was defined as grade III or IV by the classification of Papile.
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In neonatal intensive care unit, an average of up to 2 weeks of life
|
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Rate of periventricular leukomalacia
Time Frame: In neonatal intensive care unit, an average of up to 40 weeks' postmenstrual age
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Periventricular leukomalacia is diagnosed using head ultrasound or magnetic resonance imaging, typically cysts formation in the periventricular white matter.
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In neonatal intensive care unit, an average of up to 40 weeks' postmenstrual age
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Rate of necrotizing enterocolitis
Time Frame: In neonatal intensive care unit, an average of up to 2 weeks of life
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The diagnosis with necrotizing enterocolitis.
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In neonatal intensive care unit, an average of up to 2 weeks of life
|
|
Rate of sepsis
Time Frame: In neonatal intensive care unit, an average of up to 4 weeks of life
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Sepsis is defined as septicemia or bacteremia with a positive culture result of the blood and/or cerebrospinal fluid.
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In neonatal intensive care unit, an average of up to 4 weeks of life
|
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Rate of need for treatment for retinopathy of prematurity
Time Frame: In neonatal intensive care unit, an average of up to 40 weeks' postmenstrual age
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The diagnosis of retinopathy of prematurity and the decision on the need for treatment were made by ophthalmologic examination.
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In neonatal intensive care unit, an average of up to 40 weeks' postmenstrual age
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Weight
Time Frame: At 40 weeks' postmenstrual age or at discharge (approximately 40 weeks' postmenstrual age)
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Physical measurement.
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At 40 weeks' postmenstrual age or at discharge (approximately 40 weeks' postmenstrual age)
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Length
Time Frame: At 40 weeks' postmenstrual age or at discharge (approximately 40 weeks' postmenstrual age)
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Physical measurement.
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At 40 weeks' postmenstrual age or at discharge (approximately 40 weeks' postmenstrual age)
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Head circumference
Time Frame: At 40 weeks' postmenstrual age or at discharge (approximately 40 weeks' postmenstrual age)
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Physical measurement.
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At 40 weeks' postmenstrual age or at discharge (approximately 40 weeks' postmenstrual age)
|
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Postmenstrual age
Time Frame: At discharge, an average at 40 weeks' postmenstrual age
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Postmenstrual age is calculated based on their gestational age and date at birth.
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At discharge, an average at 40 weeks' postmenstrual age
|
|
Need for home oxygen therapy
Time Frame: At discharge, an average at 40 weeks' postmenstrual age
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Need for home oxygen therapy.
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At discharge, an average at 40 weeks' postmenstrual age
|
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Tracheostomy
Time Frame: In neonatal intensive care unit, an average at 40 weeks' postmenstrual age
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Need for tracheostomy.
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In neonatal intensive care unit, an average at 40 weeks' postmenstrual age
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Length of hospital stay
Time Frame: In neonatal intensive care unit, an average at 40 weeks' postmenstrual age
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The initial hospitalization.
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In neonatal intensive care unit, an average at 40 weeks' postmenstrual age
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Survival rate
Time Frame: At 3 years of age
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Survival rate is the proportion of those have survived.
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At 3 years of age
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Modified developmental quotient
Time Frame: At 3 years of age
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Modified developmental quotient is calculated by dividing developmental age (measured by the Kyoto Scale of Psychological Development) by the corrected age.
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At 3 years of age
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Rate of cerebral palsy
Time Frame: At 3 years of age
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Cerebral palsy is defined as (1) a non-progressive disorder of the central nervous system appearing in early years of life and clinically characterized by a persistent but not unchanging impairment of movement and posture and/or (2) the Gross Motor Function Classification System level ≥ II.
|
At 3 years of age
|
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Rate of visual impairment
Time Frame: At 3 years of age
|
Visual impairment is defined as unilateral or bilateral blindness, or any other condition requiring corrective lenses, which were diagnosed or determined by ophthalmologists.
|
At 3 years of age
|
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Rate of hearing impairment
Time Frame: At 3 years of age
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Hearing impairment is defined as unilateral or bilateral hearing loss that requires a hearing aid.
The diagnosis of hearing loss was made by otolaryngologists using auditory steady-state response.
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At 3 years of age
|
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Rate of those who need home oxygen therapy
Time Frame: At 3 years of age
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Need for home oxygen therapy.
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At 3 years of age
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Rate of those who need tracheostomy
Time Frame: At 3 years of age
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Need for tracheostomy.
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At 3 years of age
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Rate of those who need tube feeding or gastrostomy
Time Frame: At 3 years of age
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Need for tube feeding or gastrostomy.
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At 3 years of age
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Rate of those who need rehospitalization
Time Frame: After 18 months of corrected age unit until 3 years of age
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Need for rehospitalization.
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After 18 months of corrected age unit until 3 years of age
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Weight
Time Frame: At 3 years of age
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Physical measurement.
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At 3 years of age
|
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Height
Time Frame: At 3 years of age
|
Physical measurement.
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At 3 years of age
|
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Head circumference
Time Frame: At 3 years of age
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Physical measurement.
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At 3 years of age
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Ryo Itoshima, MD, Nagano Children's Hospital
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- summary-500g
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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