Summary of Infants Weighing 500 Grams or Less

November 18, 2024 updated by: Ryo Itoshima, Nagano Children's Hospital

Microcephaly At Birth As a Potential Predictor of Poor Prognosis in Infants Weighing 500 Grams or Less: a Retrospective Cohort Study

This is a retrospective single-center cohort study. The comparison in short- and long-term outcomes will be made between those with and without primary microcephaly in infants weighing ≤ 500 g.

Study Overview

Status

Completed

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

Observational

Enrollment (Actual)

22

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Nagano
      • Azumino, Nagano, Japan, 399-8288
        • Nagano Children's Hospital

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Sampling Method

Non-Probability Sample

Study Population

Those who were admitted to Nagano Children's Hospital NICU between January 1, 2010, and December 31, 2019.

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

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

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Microcephaly
Infants with primary microcephaly.
Those with a z score of birth head circumference < -2 (primary microcephaly) are classified into the Microcephaly group.
Control
Infants without primary microcephaly.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Rate of neurodevelopmental impairment
Time Frame: 3 years of age
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.
Survival rate is the proportion of those have survived.
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
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.
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.
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
Intraventricular hemorrhage is diagnosed by neonatologists using head ultrasound. Severe IVH was defined as grade III or IV by the classification of Papile.
In neonatal intensive care unit, an average of up to 2 weeks of life
Rate of periventricular leukomalacia
Time Frame: In neonatal intensive care unit, an average of up to 40 weeks' postmenstrual age
Periventricular leukomalacia is diagnosed using head ultrasound or magnetic resonance imaging, typically cysts formation in the periventricular white matter.
In neonatal intensive care unit, an average of up to 40 weeks' postmenstrual age
Rate of necrotizing enterocolitis
Time Frame: In neonatal intensive care unit, an average of up to 2 weeks of life
The diagnosis with necrotizing enterocolitis.
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
Sepsis is defined as septicemia or bacteremia with a positive culture result of the blood and/or cerebrospinal fluid.
In neonatal intensive care unit, an average of up to 4 weeks of life
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
The diagnosis of retinopathy of prematurity and the decision on the need for treatment were made by ophthalmologic examination.
In neonatal intensive care unit, an average of up to 40 weeks' postmenstrual age
Weight
Time Frame: At 40 weeks' postmenstrual age or at discharge (approximately 40 weeks' postmenstrual age)
Physical measurement.
At 40 weeks' postmenstrual age or at discharge (approximately 40 weeks' postmenstrual age)
Length
Time Frame: At 40 weeks' postmenstrual age or at discharge (approximately 40 weeks' postmenstrual age)
Physical measurement.
At 40 weeks' postmenstrual age or at discharge (approximately 40 weeks' postmenstrual age)
Head circumference
Time Frame: At 40 weeks' postmenstrual age or at discharge (approximately 40 weeks' postmenstrual age)
Physical measurement.
At 40 weeks' postmenstrual age or at discharge (approximately 40 weeks' postmenstrual age)
Postmenstrual age
Time Frame: At discharge, an average at 40 weeks' postmenstrual age
Postmenstrual age is calculated based on their gestational age and date at birth.
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
Need for home oxygen therapy.
At discharge, an average at 40 weeks' postmenstrual age
Tracheostomy
Time Frame: In neonatal intensive care unit, an average at 40 weeks' postmenstrual age
Need for tracheostomy.
In neonatal intensive care unit, an average at 40 weeks' postmenstrual age
Length of hospital stay
Time Frame: In neonatal intensive care unit, an average at 40 weeks' postmenstrual age
The initial hospitalization.
In neonatal intensive care unit, an average at 40 weeks' postmenstrual age
Survival rate
Time Frame: At 3 years of age
Survival rate is the proportion of those have survived.
At 3 years of age
Modified developmental quotient
Time Frame: At 3 years of age
Modified developmental quotient is calculated by dividing developmental age (measured by the Kyoto Scale of Psychological Development) by the corrected age.
At 3 years of age
Rate of cerebral palsy
Time Frame: At 3 years of age
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
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
Rate of hearing impairment
Time Frame: At 3 years of age
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.
At 3 years of age
Rate of those who need home oxygen therapy
Time Frame: At 3 years of age
Need for home oxygen therapy.
At 3 years of age
Rate of those who need tracheostomy
Time Frame: At 3 years of age
Need for tracheostomy.
At 3 years of age
Rate of those who need tube feeding or gastrostomy
Time Frame: At 3 years of age
Need for tube feeding or gastrostomy.
At 3 years of age
Rate of those who need rehospitalization
Time Frame: After 18 months of corrected age unit until 3 years of age
Need for rehospitalization.
After 18 months of corrected age unit until 3 years of age
Weight
Time Frame: At 3 years of age
Physical measurement.
At 3 years of age
Height
Time Frame: At 3 years of age
Physical measurement.
At 3 years of age
Head circumference
Time Frame: At 3 years of age
Physical measurement.
At 3 years of age

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Ryo Itoshima, MD, Nagano Children's Hospital

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

April 5, 2022

Primary Completion (Actual)

December 31, 2022

Study Completion (Actual)

December 31, 2022

Study Registration Dates

First Submitted

March 4, 2022

First Submitted That Met QC Criteria

April 4, 2022

First Posted (Actual)

April 12, 2022

Study Record Updates

Last Update Posted (Estimated)

November 20, 2024

Last Update Submitted That Met QC Criteria

November 18, 2024

Last Verified

November 1, 2024

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

No

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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